JPS6450879A - Production of thianaphthene derivative - Google Patents
Production of thianaphthene derivativeInfo
- Publication number
- JPS6450879A JPS6450879A JP62207562A JP20756287A JPS6450879A JP S6450879 A JPS6450879 A JP S6450879A JP 62207562 A JP62207562 A JP 62207562A JP 20756287 A JP20756287 A JP 20756287A JP S6450879 A JPS6450879 A JP S6450879A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- solvent
- vilsmeier reagent
- dimethylformamide
- 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.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
PURPOSE:To obtain a thianaphthene useful as a synthetic intermediate for a compound having antithrombotic action readily and in high yield, by reacting a specific compound as a raw material with a Vilsmeier reagent. CONSTITUTION:A thiophene derivative shown by formula II [R1-R3 are H, lower alkyl or (substituted)aryl; R4 is carboxyl-protecting group] is reacted with a Vilsmeier reagent such as dimethylformamide and phosphorus oxychloride in a solvent such as methylene chloride to give a compound shown by formula III. This compound is subjected to ring closure in a solvent such as toluene in the presence of a base such as NaH to form a specific compound shown by formula IV as a raw material. The compound is further reacted with the same Vilsmeier reagent as the above-mentioned reagent in a solvent such as dimethylformamide to give the aimed compound shown by formula I useful as a synthetic intermediate for sodium 6-[4,5-dihydro-2-(1-imidazolyl) methylthianaphthene]carboxylate having excellent antithrombotic action.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62207562A JPH0613504B2 (en) | 1987-08-21 | 1987-08-21 | Method for producing thianaphthene derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62207562A JPH0613504B2 (en) | 1987-08-21 | 1987-08-21 | Method for producing thianaphthene derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6450879A true JPS6450879A (en) | 1989-02-27 |
JPH0613504B2 JPH0613504B2 (en) | 1994-02-23 |
Family
ID=16541795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62207562A Expired - Lifetime JPH0613504B2 (en) | 1987-08-21 | 1987-08-21 | Method for producing thianaphthene derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0613504B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999064425A1 (en) * | 1998-06-09 | 1999-12-16 | Neurogen Corporation | Substituted thienocycloalkylpyrazoles: dopamine receptor subtype specific ligands |
-
1987
- 1987-08-21 JP JP62207562A patent/JPH0613504B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999064425A1 (en) * | 1998-06-09 | 1999-12-16 | Neurogen Corporation | Substituted thienocycloalkylpyrazoles: dopamine receptor subtype specific ligands |
Also Published As
Publication number | Publication date |
---|---|
JPH0613504B2 (en) | 1994-02-23 |
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