GB1410162A - 2-aminoindane derivatives - Google Patents
2-aminoindane derivativesInfo
- Publication number
- GB1410162A GB1410162A GB897574A GB897574A GB1410162A GB 1410162 A GB1410162 A GB 1410162A GB 897574 A GB897574 A GB 897574A GB 897574 A GB897574 A GB 897574A GB 1410162 A GB1410162 A GB 1410162A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon atoms
- formula
- group
- radical containing
- march
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- LMHHFZAXSANGGM-UHFFFAOYSA-N 2-aminoindane Chemical class C1=CC=C2CC(N)CC2=C1 LMHHFZAXSANGGM-UHFFFAOYSA-N 0.000 title abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- CFIDFVNAHVRFGT-UHFFFAOYSA-N 2,3-dihydro-1h-inden-2-yl methanesulfonate Chemical compound C1=CC=C2CC(OS(=O)(=O)C)CC2=C1 CFIDFVNAHVRFGT-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- 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
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1410162 2-Aminoindanes MANUFACTURE DE PRODUITS PHARMACEUTIQUES A CHRISTIAENS SA 1 March 1974 [1 March 1973] 8975/74 Divided out of 1405444 Heading C2C Compounds of Formula I wherein n is equal 2 or 3, the (CH 2 ) n group having a straight or branched chain; R 1 and R 2 each represents a lower alkyl radical containing 1 to 3 carbon atoms, whereby R 1 and R 2 may also form together with the adjacent nitrogen atom a nitrogenous heterocyclic ring; A represents a phenyl group optionally substituted in the ortho, meta and/or para position by at least one substituent selected from an alkyl or alkoxy group containing from 1 to 4 carbon atoms, a hydroxy, trifluoromethyl, halo and a nitro group; and B represents a hydrogen atom, an alkoxy radical containing 1 to 3 carbon atoms or a group of the formula in which R 3 and R 4 , which may be identical or different, each represents a lower alkyl or hydroxyalkyl radical containing from 1 to 4 carbon atoms, whereby R 3 may also represent hydrogen, whereas R 3 and R 4 may also form, with the attached nitrogen atom, a nitrogenous heterocyclic ring; as well as the acid addition salts of said compounds, are prepared by the reaction of a 2-indanol mesylate of Formula (II), with a compound of Formula III Reference has been directed by the Comptroller to Specification 1,321,424.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB897574A GB1410162A (en) | 1973-03-01 | 1973-03-01 | 2-aminoindane derivatives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB897574A GB1410162A (en) | 1973-03-01 | 1973-03-01 | 2-aminoindane derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1410162A true GB1410162A (en) | 1975-10-15 |
Family
ID=9862930
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB897574A Expired GB1410162A (en) | 1973-03-01 | 1973-03-01 | 2-aminoindane derivatives |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1410162A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT380682B (en) * | 1981-03-04 | 1986-06-25 | Alkaloida Vegyeszeti Gyar | METHOD FOR PRODUCING NEW ALKYLENE DIAMINE DERIVATIVES |
-
1973
- 1973-03-01 GB GB897574A patent/GB1410162A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT380682B (en) * | 1981-03-04 | 1986-06-25 | Alkaloida Vegyeszeti Gyar | METHOD FOR PRODUCING NEW ALKYLENE DIAMINE DERIVATIVES |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |