SK10182000A3 - Spôsob výroby ketimínu - Google Patents

Spôsob výroby ketimínu Download PDF

Info

Publication number: SK10182000A3
Authority: SK; Slovakia
Prior art keywords: sertraline; cis; mixture; trans; solvent
Prior art date: 1998-01-16

Application number

SK1018-2000A

Other languages

English (en)

Slovak (sk)

Inventor

Juan Carlos Colberg

David Michael Pfisterer

Geraldine Patricia Taber

Original Assignee

Pfizer Products Inc.

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-01-16

Filing date

1998-10-15

Publication date

2002-06-04

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22102365&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK10182000(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1998-10-15 Application filed by Pfizer Products Inc. filed Critical Pfizer Products Inc.

2002-06-04 Publication of SK10182000A3 publication Critical patent/SK10182000A3/sk

Links

150000004658 ketimines Chemical class 0.000 title claims description 21
238000004519 manufacturing process Methods 0.000 title claims description 12
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims abstract description 84
238000000034 method Methods 0.000 claims abstract description 51
230000008569 process Effects 0.000 claims abstract description 40
JGMBHJNMQVKDMW-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-3,4-dihydro-2h-naphthalen-1-one Chemical compound C1=C(Cl)C(Cl)=CC=C1C1C2=CC=CC=C2C(=O)CC1 JGMBHJNMQVKDMW-UHFFFAOYSA-N 0.000 claims abstract description 15
MGBVAZJASCWJGJ-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-n-methyl-3,4-dihydro-2h-naphthalen-1-imine Chemical compound C12=CC=CC=C2C(=NC)CCC1C1=CC=C(Cl)C(Cl)=C1 MGBVAZJASCWJGJ-UHFFFAOYSA-N 0.000 claims abstract description 15
238000002360 preparation method Methods 0.000 claims abstract description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 61
229960002073 sertraline Drugs 0.000 claims description 53
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 51
239000000203 mixture Substances 0.000 claims description 43
238000006243 chemical reaction Methods 0.000 claims description 42
VGKDLMBJGBXTGI-SJCJKPOMSA-N sertraline Chemical compound C1([C@@H]2CC[C@@H](C3=CC=CC=C32)NC)=CC=C(Cl)C(Cl)=C1 VGKDLMBJGBXTGI-SJCJKPOMSA-N 0.000 claims description 41
239000002904 solvent Substances 0.000 claims description 37
XHLHPRDBBAGVEG-UHFFFAOYSA-N 1-tetralone Chemical compound C1=CC=C2C(=O)CCCC2=C1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 claims description 28
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 26
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 20
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 14
239000003054 catalyst Substances 0.000 claims description 13
238000005984 hydrogenation reaction Methods 0.000 claims description 11
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 10
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 10
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 9
150000001298 alcohols Chemical class 0.000 claims description 9
238000009835 boiling Methods 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 7
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
230000001476 alcoholic effect Effects 0.000 claims description 6
229910052799 carbon Inorganic materials 0.000 claims description 6
-1 n-pro-panol Natural products 0.000 claims description 6
VGKDLMBJGBXTGI-SJKOYZFVSA-N (1r,4r)-4-(3,4-dichlorophenyl)-n-methyl-1,2,3,4-tetrahydronaphthalen-1-amine Chemical compound C1([C@H]2CC[C@H](C3=CC=CC=C32)NC)=CC=C(Cl)C(Cl)=C1 VGKDLMBJGBXTGI-SJKOYZFVSA-N 0.000 claims description 5
235000019445 benzyl alcohol Nutrition 0.000 claims description 4
238000011065 in-situ storage Methods 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims 1
229960005335 propanol Drugs 0.000 claims 1
239000000047 product Substances 0.000 description 18
229910052739 hydrogen Inorganic materials 0.000 description 16
239000001257 hydrogen Substances 0.000 description 16
239000011541 reaction mixture Substances 0.000 description 16
230000015572 biosynthetic process Effects 0.000 description 14
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 11
238000001914 filtration Methods 0.000 description 11
239000012458 free base Substances 0.000 description 11
238000001953 recrystallisation Methods 0.000 description 11
238000003786 synthesis reaction Methods 0.000 description 11
150000002466 imines Chemical class 0.000 description 10
IWYDHOAUDWTVEP-UHFFFAOYSA-M mandelate Chemical class [O-]C(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-M 0.000 description 9
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 8
239000000543 intermediate Substances 0.000 description 8
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 8
MGBVAZJASCWJGJ-LBPRGKRZSA-N (4s)-4-(3,4-dichlorophenyl)-n-methyl-3,4-dihydro-2h-naphthalen-1-imine Chemical compound C1([C@@H]2CCC(C3=CC=CC=C32)=NC)=CC=C(Cl)C(Cl)=C1 MGBVAZJASCWJGJ-LBPRGKRZSA-N 0.000 description 7
239000006227 byproduct Substances 0.000 description 7
239000003610 charcoal Substances 0.000 description 7
239000002808 molecular sieve Substances 0.000 description 7
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
230000003197 catalytic effect Effects 0.000 description 5
238000006482 condensation reaction Methods 0.000 description 5
238000004821 distillation Methods 0.000 description 5
230000001965 increasing effect Effects 0.000 description 5
238000006268 reductive amination reaction Methods 0.000 description 5
230000002829 reductive effect Effects 0.000 description 5
229960003660 sertraline hydrochloride Drugs 0.000 description 5
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 5
GLQPTZAAUROJMO-UHFFFAOYSA-N 4-(3,4-dimethoxyphenyl)benzaldehyde Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC=C(C=O)C=C1 GLQPTZAAUROJMO-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
239000003245 coal Substances 0.000 description 4
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
239000007858 starting material Substances 0.000 description 4
QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000002955 isolation Methods 0.000 description 3
229960002510 mandelic acid Drugs 0.000 description 3
NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000004408 titanium dioxide Substances 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
238000006073 displacement reaction Methods 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 2
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
238000006722 reduction reaction Methods 0.000 description 2
238000010992 reflux Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
238000000926 separation method Methods 0.000 description 2
238000010583 slow cooling Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
RZPFVRFSYMUDJO-UHFFFAOYSA-N 2h-naphthalen-1-one Chemical compound C1=CC=C2C(=O)CC=CC2=C1 RZPFVRFSYMUDJO-UHFFFAOYSA-N 0.000 description 1
VGKDLMBJGBXTGI-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-n-methyl-1,2,3,4-tetrahydronaphthalen-1-amine Chemical compound C12=CC=CC=C2C(NC)CCC1C1=CC=C(Cl)C(Cl)=C1 VGKDLMBJGBXTGI-UHFFFAOYSA-N 0.000 description 1
IXLVUUFUDRJUSL-RPBOFIJWSA-N 5-[[4-(3-acetamidophenyl)phenyl]methyl]-n-[(1s,2r)-2-phenylcyclopropyl]-1,3-oxazole-4-carboxamide Chemical compound CC(=O)NC1=CC=CC(C=2C=CC(CC3=C(N=CO3)C(=O)N[C@@H]3[C@H](C3)C=3C=CC=CC=3)=CC=2)=C1 IXLVUUFUDRJUSL-RPBOFIJWSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000001430 anti-depressive effect Effects 0.000 description 1
239000000935 antidepressant agent Substances 0.000 description 1
229940005513 antidepressants Drugs 0.000 description 1
150000003938 benzyl alcohols Chemical class 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
239000012024 dehydrating agents‎ Substances 0.000 description 1
238000006356 dehydrogenation reaction Methods 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
239000010439 graphite Substances 0.000 description 1
239000002638 heterogeneous catalyst Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
238000009776 industrial production Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910000510 noble metal Inorganic materials 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
239000011148 porous material Substances 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
238000010956 selective crystallization Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003509 tertiary alcohols Chemical class 0.000 description 1
230000035899 viability Effects 0.000 description 1
229940020965 zoloft Drugs 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/02—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of compounds containing imino groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Cephalosporin Compounds (AREA)
Steroid Compounds (AREA)

SK1018-2000A 1998-01-16 1998-10-15 Spôsob výroby ketimínu SK10182000A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US7160098P	1998-01-16	1998-01-16
PCT/IB1998/001619 WO1999036394A1 (fr)	1998-01-16	1998-10-15	Nouveau procede de preparation d'une ketimine

Publications (1)

Publication Number	Publication Date
SK10182000A3 true SK10182000A3 (sk)	2002-06-04

Family

ID=22102365

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1018-2000A SK10182000A3 (sk)	1998-01-16	1998-10-15	Spôsob výroby ketimínu

Country Status (47)

Country	Link
US (1)	US6232500B1 (fr)
EP (1)	EP1047666B1 (fr)
JP (1)	JP3533179B2 (fr)
KR (1)	KR100362788B1 (fr)
CN (1)	CN1121381C (fr)
AP (1)	AP956A (fr)
AR (1)	AR016168A1 (fr)
AT (1)	ATE231121T1 (fr)
AU (1)	AU747861B2 (fr)
BG (2)	BG64621B1 (fr)
BR (1)	BR9814248A (fr)
CA (1)	CA2315761C (fr)
CO (1)	CO5040154A1 (fr)
CZ (1)	CZ20002594A3 (fr)
DE (1)	DE69810815T2 (fr)
DK (1)	DK1047666T3 (fr)
DZ (1)	DZ2705A1 (fr)
EA (1)	EA004952B1 (fr)
EG (1)	EG21515A (fr)
ES (1)	ES2186226T3 (fr)
GT (1)	GT199800176A (fr)
HN (1)	HN1998000167A (fr)
HR (1)	HRP20000473A2 (fr)
HU (1)	HUP0101253A3 (fr)
ID (1)	ID24971A (fr)
IL (2)	IL136888A0 (fr)
IN (1)	IN191358B (fr)
IS (1)	IS5538A (fr)
MA (1)	MA24744A1 (fr)
MY (1)	MY132956A (fr)
NO (1)	NO20003625L (fr)
NZ (1)	NZ505027A (fr)
OA (1)	OA11439A (fr)
PA (1)	PA8461901A1 (fr)
PE (1)	PE20000171A1 (fr)
PL (1)	PL192489B1 (fr)
PT (1)	PT1047666E (fr)
RS (1)	RS49773B (fr)
SI (1)	SI1047666T1 (fr)
SK (1)	SK10182000A3 (fr)
TN (1)	TNSN99004A1 (fr)
TR (1)	TR200002065T2 (fr)
TW (1)	TW505624B (fr)
UA (1)	UA55504C2 (fr)
UY (1)	UY25348A1 (fr)
WO (1)	WO1999036394A1 (fr)
ZA (1)	ZA99278B (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU226423B1 (en) *	1998-05-05	2008-12-29	Egis Gyogyszergyar Nyrt	Process for producing a 1(2h)-naphtalene-1-ylidene derivative
IL142367A0 (en) *	1998-10-30	2002-03-10	Ciba Sc Holding Ag	Method of producing ketimines
EP1630156A1 (fr) *	1998-11-27	2006-03-01	Teva Pharmaceutical Industries Ltd	Polymorphes de chlorhydrate de Sertraline
IN185109B (fr) *	1999-09-01	2000-11-18	Torrent Pharmaceuticals Ltd
EP1230212B1 (fr) *	1999-11-16	2005-05-11	Ciba SC Holding AG	Procede de preparation de cetimines
EP1230211B1 (fr) *	1999-11-16	2005-07-20	Ciba SC Holding AG	Procede de preparation de cetimines
IN187170B (fr)	2000-01-04	2002-02-23	Sun Pharmaceutical Ind Ltd
SK14212002A3 (sk) *	2000-03-14	2003-07-01	Teva Pharmaceutical Industries Ltd.	Spôsob prípravy (+)-cis-sertralínu
WO2002096860A1 (fr) *	2001-05-31	2002-12-05	Orion Corporation Fermion	Procede de preparation d'intermediaires de sertraline
US6723878B2 (en)	2001-06-15	2004-04-20	Orion Corporation Fermion	Method for preparing sertraline
KR20030061474A (ko) *	2002-01-14	2003-07-22	한미약품 주식회사	서트랄린 제조용 중간체로서 사용되는 시스-라세메이트화합물의 개선된 제조방법
CA2576097C (fr)	2005-06-03	2009-10-27	Hetero Drugs Limited	Synthese hautement stereoselective de sertraline

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4536518A (en)	1979-11-01	1985-08-20	Pfizer Inc.	Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine
US4855500A (en) *	1988-05-04	1989-08-08	Pfizer Inc.	Process for preparing a ketimine
HU226424B1 (en)	1998-05-05	2008-12-29	Egis Gyogyszergyar Nyrt	Process for producing enantiomer mixture for preparation of sertraline

1998
- 1998-06-24 IN IN8499DE1998 patent/IN191358B/en unknown
- 1998-10-15 HU HU0101253A patent/HUP0101253A3/hu unknown
- 1998-10-15 BR BR9814248-8A patent/BR9814248A/pt not_active Application Discontinuation
- 1998-10-15 AT AT98945508T patent/ATE231121T1/de not_active IP Right Cessation
- 1998-10-15 CN CN98813087A patent/CN1121381C/zh not_active Expired - Fee Related
- 1998-10-15 US US09/380,562 patent/US6232500B1/en not_active Expired - Fee Related
- 1998-10-15 AU AU92786/98A patent/AU747861B2/en not_active Ceased
- 1998-10-15 JP JP2000540112A patent/JP3533179B2/ja not_active Expired - Fee Related
- 1998-10-15 WO PCT/IB1998/001619 patent/WO1999036394A1/fr not_active Ceased
- 1998-10-15 HR HR20000473A patent/HRP20000473A2/hr not_active Application Discontinuation
- 1998-10-15 KR KR1020007007730A patent/KR100362788B1/ko not_active Expired - Fee Related
- 1998-10-15 NZ NZ505027A patent/NZ505027A/xx unknown
- 1998-10-15 ID IDW20001367A patent/ID24971A/id unknown
- 1998-10-15 CZ CZ20002594A patent/CZ20002594A3/cs unknown
- 1998-10-15 SI SI9830331T patent/SI1047666T1/xx unknown
- 1998-10-15 CA CA002315761A patent/CA2315761C/fr not_active Expired - Fee Related
- 1998-10-15 TR TR2000/02065T patent/TR200002065T2/xx unknown
- 1998-10-15 RS YUP-443/00A patent/RS49773B/sr unknown
- 1998-10-15 DK DK98945508T patent/DK1047666T3/da active
- 1998-10-15 IL IL13688898A patent/IL136888A0/xx active IP Right Grant
- 1998-10-15 EP EP98945508A patent/EP1047666B1/fr not_active Revoked
- 1998-10-15 ES ES98945508T patent/ES2186226T3/es not_active Expired - Lifetime
- 1998-10-15 EA EA200000661A patent/EA004952B1/ru not_active IP Right Cessation
- 1998-10-15 SK SK1018-2000A patent/SK10182000A3/sk unknown
- 1998-10-15 PL PL341648A patent/PL192489B1/pl not_active IP Right Cessation
- 1998-10-15 DE DE69810815T patent/DE69810815T2/de not_active Revoked
- 1998-10-15 UA UA2000074225A patent/UA55504C2/uk unknown
- 1998-10-15 PT PT98945508T patent/PT1047666E/pt unknown
- 1998-10-22 PA PA19988461901A patent/PA8461901A1/es unknown
- 1998-10-26 HN HN1998000167A patent/HN1998000167A/es unknown
- 1998-11-09 GT GT199800176A patent/GT199800176A/es unknown
- 1998-11-30 CO CO98070715A patent/CO5040154A1/es unknown
1999
- 1999-01-11 EG EG2799A patent/EG21515A/xx active
- 1999-01-11 PE PE1999000023A patent/PE20000171A1/es not_active Application Discontinuation
- 1999-01-13 MY MYPI99000116A patent/MY132956A/en unknown
- 1999-01-13 MA MA25427A patent/MA24744A1/fr unknown
- 1999-01-13 UY UY25348A patent/UY25348A1/es not_active IP Right Cessation
- 1999-01-13 TW TW088100478A patent/TW505624B/zh not_active IP Right Cessation
- 1999-01-13 DZ DZ990006A patent/DZ2705A1/fr active
- 1999-01-13 TN TNTNSN99004A patent/TNSN99004A1/fr unknown
- 1999-01-14 AP APAP/P/1999/001441A patent/AP956A/en active
- 1999-01-15 AR ARP990100129A patent/AR016168A1/es active IP Right Grant
- 1999-01-15 ZA ZA9900278A patent/ZA99278B/xx unknown
2000
- 2000-06-16 IS IS5538A patent/IS5538A/is unknown
- 2000-06-19 IL IL136888A patent/IL136888A/en not_active IP Right Cessation
- 2000-06-30 OA OA1200000193A patent/OA11439A/en unknown
- 2000-07-14 NO NO20003625A patent/NO20003625L/no not_active Application Discontinuation
- 2000-08-07 BG BG104669A patent/BG64621B1/bg unknown
- 2000-08-07 BG BG108878A patent/BG64647B1/bg unknown

Also Published As

Publication number	Publication date
RS49773B (sr)	2008-06-05
AP9901441A0 (en)	1999-03-31
CN1285819A (zh)	2001-02-28
TW505624B (en)	2002-10-11
NO20003625D0 (no)	2000-07-14
UA55504C2 (uk)	2003-04-15
BG104669A (en)	2001-04-30
AU9278698A (en)	1999-08-02
ATE231121T1 (de)	2003-02-15
CN1121381C (zh)	2003-09-17
DK1047666T3 (da)	2003-02-24
HK1032039A1 (en)	2001-07-06
PL192489B1 (pl)	2006-10-31
PL341648A1 (en)	2001-04-23
HUP0101253A3 (en)	2002-06-28
JP2002509132A (ja)	2002-03-26
KR100362788B1 (ko)	2002-11-29
PT1047666E (pt)	2003-03-31
ZA99278B (en)	2000-07-17
CZ20002594A3 (cs)	2001-12-12
JP3533179B2 (ja)	2004-05-31
BG64647B1 (bg)	2005-10-31
BR9814248A (pt)	2000-10-10
EA004952B1 (ru)	2004-10-28
KR20010034117A (ko)	2001-04-25
MA24744A1 (fr)	1999-10-01
CA2315761A1 (fr)	1999-07-22
ID24971A (id)	2000-08-31
HUP0101253A2 (hu)	2002-05-29
AP956A (en)	2001-04-06
UY25348A1 (es)	1999-09-27
IL136888A0 (en)	2001-06-14
SI1047666T1 (en)	2003-04-30
DZ2705A1 (fr)	2003-09-01
EA200000661A1 (ru)	2000-12-25
YU44300A (sh)	2002-09-19
IS5538A (is)	2000-06-16
EG21515A (en)	2001-11-28
MY132956A (en)	2007-10-31
CA2315761C (fr)	2004-08-31
NZ505027A (en)	2002-08-28
OA11439A (en)	2004-04-26
NO20003625L (no)	2000-09-13
US6232500B1 (en)	2001-05-15
BG64621B1 (bg)	2005-09-30
CO5040154A1 (es)	2001-05-29
EP1047666A1 (fr)	2000-11-02
IL136888A (en)	2006-12-10
HN1998000167A (es)	1999-02-09
ES2186226T3 (es)	2003-05-01
GT199800176A (es)	1998-11-09
PE20000171A1 (es)	2000-03-09
DE69810815T2 (de)	2003-08-07
IN191358B (fr)	2003-11-29
DE69810815D1 (de)	2003-02-20
TNSN99004A1 (fr)	2005-11-10
HRP20000473A2 (en)	2001-04-30
EP1047666B1 (fr)	2003-01-15
TR200002065T2 (tr)	2000-11-21
AR016168A1 (es)	2001-06-20
PA8461901A1 (es)	2000-05-24
WO1999036394A1 (fr)	1999-07-22
AU747861B2 (en)	2002-05-23

Publication	Publication Date	Title
US7563931B2 (en)	2009-07-21	Process for preparation of phenethylamine derivatives
SK10182000A3 (sk)	2002-06-04	Spôsob výroby ketimínu
EP2403823B1 (fr)	2015-10-21	Procédé de préparation de cinacalcet et de ses sels, et intermédiaires destinés à être utilisés dans le procédé
RU2181358C2 (ru)	2002-04-20	Способ получения сертралина из хирального тетралона
WO2001016089A1 (fr)	2001-03-08	Procede de preparation de chlorhydrate de cis-(1s,4s)-n-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthaleneamine
US20130150622A1 (en)	2013-06-13	Stereoselective synthesis of tapentadol and its salts
CA2448499A1 (fr)	2002-12-27	Nouveau procede pour la preparation de (is-cis)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-n-methyl-1-naphtalenamine
MXPA00006986A (en)	2001-07-03	Novel process for preparing a ketimine
HK1032039B (en)	2004-01-16	Novel process for preparing a ketimine
EP1238965B1 (fr)	2005-06-08	Procédé de préparation du 1-(2-diméthylamino-(4-méthoxyphényl)-éthyl)cyclohexanol
US6723878B2 (en)	2004-04-20	Method for preparing sertraline
WO2006067808A1 (fr)	2006-06-29	Procede ameliore pour la production d’un intermediaire d’un agent antidepresseur
JP4049544B2 (ja)	2008-02-20	光学活性１−（フルオロフェニル）エチルアミンの製造方法
WO2012098044A1 (fr)	2012-07-26	Procédé pour la préparation de n,n-diisopropyl-3-(2-hydroxy-5-méthylphényl)-3-phénylpropylamine et de ses sels à partir d'un nouvel intermédiaire
EA009659B1 (ru)	2008-02-28	Способ получения иминного промежуточного соединения
EP2476665A1 (fr)	2012-07-18	Procédé pour la préparation de N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)- 3-phenyl propylamine et ses sels démarrant à partir d'un nouvel intermédiaire