GB1311260A - Process for producing imidazo 2,1-a isoindoles - Google Patents
Process for producing imidazo 2,1-a isoindolesInfo
- Publication number
- GB1311260A GB1311260A GB3670272A GB3670272A GB1311260A GB 1311260 A GB1311260 A GB 1311260A GB 3670272 A GB3670272 A GB 3670272A GB 3670272 A GB3670272 A GB 3670272A GB 1311260 A GB1311260 A GB 1311260A
- Authority
- GB
- United Kingdom
- Prior art keywords
- free base
- resulting
- general formula
- isoindoles
- salification
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/22—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1311260 Imidazoline derivatives SANDOZ Ltd 23 Feb 1970 [19 May 1969] 36702/72 Divided out of 1306511 Heading C2C Novel imidazoline derivatives of the general formula wherein each of R and R 1 is a hydrogen, fluorine or chlorine atom, and acid addition salts thereof are prepared by reaction of the N 1 o-dilithium derivative of 2-phenyl-2-imidazoline with a benzonitrile of the general formula under an inert atmosphere and in an organic solvent which is inert under the reaction conditions, and hydrolysis of the resulting adduct, followed optionally by salification of a resulting free base or conversion of a resulting salt into the corresponding free base. They may be converted to 5-phenyl-5-hydroxy-2,3-dihydro- 5H-imidazo[2,1-a]-isoindoles of the general formula and acid addition salts thereof by treatment with water in the presence of an acid at pH 1-4, followed optionally by salification of a resulting free base or conversion of a resulting salt into the corresponding free base.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US82595469A | 1969-05-19 | 1969-05-19 | |
US86517969A | 1969-10-09 | 1969-10-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1311260A true GB1311260A (en) | 1973-03-28 |
Family
ID=27124962
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3670272A Expired GB1311260A (en) | 1969-05-19 | 1970-02-23 | Process for producing imidazo 2,1-a isoindoles |
Country Status (2)
Country | Link |
---|---|
CH (1) | CH531510A (en) |
GB (1) | GB1311260A (en) |
-
1970
- 1970-02-20 CH CH1572472A patent/CH531510A/en not_active IP Right Cessation
- 1970-02-23 GB GB3670272A patent/GB1311260A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
CH531510A (en) | 1972-12-15 |
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