ES424221A2 - Procedure for preparation of new oxazine (5,6, e) indoles substitute. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for preparation of new oxazine (5,6, e) indoles substitute. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES424221A2 ES424221A2 ES424221A ES424221A ES424221A2 ES 424221 A2 ES424221 A2 ES 424221A2 ES 424221 A ES424221 A ES 424221A ES 424221 A ES424221 A ES 424221A ES 424221 A2 ES424221 A2 ES 424221A2
- Authority
- ES
- Spain
- Prior art keywords
- formula
- translation
- procedure
- preparation
- machine
- 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
- 150000002475 indoles Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 title 1
- -1 alcohol radical Chemical class 0.000 abstract 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- LMIQERWZRIFWNZ-UHFFFAOYSA-N 5-hydroxyindole Chemical compound OC1=CC=C2NC=CC2=C1 LMIQERWZRIFWNZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003158 alcohol group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Improvements introduced in the object of the main patent No. 403,547 applied for on June 6, 1972 by: "Procedure for the Preparation of new oxazino (5,6, e) substituted indoles, according to which when said compounds respond to the general formula: **(See formula)** in which: R1 designates an alcohol radical containing a maximum of four carbon atoms, and R2 represents an alcohol chain possibly substituted by a dialeohylamino group or by a heterocyclic radical, selected from the pyrrolidine and morpholino radicals, however, not being able, R2 signifies an ethyl, propyl or diethylaminoethyl radical when R1 symbolizes the ethyl group; Said improvements are characterized by reacting a methyl-2-alkoxycarbonyl-3 hydroxy-5-indole of formula (II): **(See formula)** with a primary amine of formula: R2NH2 (III) and an excess of formalin, with the symbols R1 and R2 in formulas (II) and (III), having the same significance as in formula (I). (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES403547A ES403547A1 (en) | 1971-06-08 | 1972-06-06 | Novel substituted oxazino(5,6,e)indoles |
| FR7310202A FR2222086B2 (en) | 1973-03-21 | 1973-03-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES424221A2 true ES424221A2 (en) | 1976-05-16 |
Family
ID=9116661
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES424221A Expired ES424221A2 (en) | 1972-06-06 | 1974-03-13 | Procedure for preparation of new oxazine (5,6, e) indoles substitute. (Machine-translation by Google Translate, not legally binding) |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JPS49126698A (en) |
| BE (1) | BE811263R (en) |
| CA (1) | CA1016546A (en) |
| CH (1) | CH560704A5 (en) |
| DE (2) | DE2462471A1 (en) |
| ES (1) | ES424221A2 (en) |
| FR (1) | FR2222086B2 (en) |
| GB (1) | GB1417381A (en) |
| IT (1) | IT1059819B (en) |
| LU (1) | LU69436A1 (en) |
| NL (1) | NL7403863A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2323221C9 (en) * | 2006-05-23 | 2010-03-27 | Андрей Александрович Иващенко | SUBSTITUTED ESTERS OF 1,2,3,7-TETRAHYDROPYRROLO[3,2-f][1,3]BENZOXAZIN-5-CARBOXYLIC ACIDS, PHARMACEUTICAL COMPOSITION, METHOD FOR THEIR PREPARING (VARIANTS) AND USING |
| WO2007136300A2 (en) | 2006-05-23 | 2007-11-29 | Alla Chem, Llc | Substituted indoles and a method for the production and use thereof |
-
1973
- 1973-03-21 FR FR7310202A patent/FR2222086B2/fr not_active Expired
-
1974
- 1974-02-14 GB GB670874A patent/GB1417381A/en not_active Expired
- 1974-02-19 BE BE141119A patent/BE811263R/en active
- 1974-02-21 LU LU69436A patent/LU69436A1/xx unknown
- 1974-02-22 DE DE19742462471 patent/DE2462471A1/en not_active Ceased
- 1974-02-22 DE DE19742408603 patent/DE2408603A1/en active Pending
- 1974-03-13 ES ES424221A patent/ES424221A2/en not_active Expired
- 1974-03-15 IT IT67788/74A patent/IT1059819B/en active
- 1974-03-18 JP JP49030164A patent/JPS49126698A/ja active Pending
- 1974-03-20 CA CA195,492A patent/CA1016546A/en not_active Expired
- 1974-03-21 NL NL7403863A patent/NL7403863A/xx not_active Application Discontinuation
- 1974-03-21 CH CH394574A patent/CH560704A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE2462471A1 (en) | 1977-05-26 |
| GB1417381A (en) | 1975-12-10 |
| LU69436A1 (en) | 1974-09-25 |
| IT1059819B (en) | 1982-06-21 |
| NL7403863A (en) | 1974-09-24 |
| JPS49126698A (en) | 1974-12-04 |
| FR2222086A2 (en) | 1974-10-18 |
| BE811263R (en) | 1974-08-19 |
| CH560704A5 (en) | 1975-04-15 |
| FR2222086B2 (en) | 1976-04-09 |
| CA1016546A (en) | 1977-08-30 |
| DE2408603A1 (en) | 1974-09-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD2A | Announcement of lapse in spain |
Effective date: 20170705 |