GB1022031A - Improvements in or relating to basic esters of 3,5-dimethoxy-4-alkoxy-benzoic acids - Google Patents
Improvements in or relating to basic esters of 3,5-dimethoxy-4-alkoxy-benzoic acidsInfo
- Publication number
- GB1022031A GB1022031A GB15974/63A GB1597463A GB1022031A GB 1022031 A GB1022031 A GB 1022031A GB 15974/63 A GB15974/63 A GB 15974/63A GB 1597463 A GB1597463 A GB 1597463A GB 1022031 A GB1022031 A GB 1022031A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethoxy
- alkoxy
- benzoic acid
- ester
- acid
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises compounds of the formula <FORM:1022031/C2/1> wherein R represents a saturated or unsaturated straight or branched chain C2- 5 alkyl group which may be substituted by a basic nitrogen-containing group of R1 and R2 represent identical or different straight or branched chain saturated alkyl groups, or the groups R1 and R2, together with the nitrogen atom to which they are attached, form a heterocyclic group which may be interrupted by a further hetero atom, and n = 2 or 3. The compounds are prepared by reacting a 3,5-dimethoxy-4-alkoxy-benzoic acid or a reactive derivative thereof, with a basic alcohol of the formula <FORM:1022031/C2/2> or with a reactive derivative thereof. 3,5 - Dimethoxy - 4 - alkoxy - benzoic acid chlorides are prepared by alkylating a 3,5-dimethoxy-4-hydroxy-benzoic acid or an ester thereof to form a 3,5-dimethoxy-4-alkoxy-benzoic acid or an ester thereof, followed, if necessary by hydrolysis of the ester to form the free acid, and reacting the free acid with thionyl chloride to form the acid chloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HUGO000856 | 1962-05-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1022031A true GB1022031A (en) | 1966-03-09 |
Family
ID=10996637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15974/63A Expired GB1022031A (en) | 1962-05-11 | 1963-04-23 | Improvements in or relating to basic esters of 3,5-dimethoxy-4-alkoxy-benzoic acids |
Country Status (4)
Country | Link |
---|---|
CS (1) | CS160625B2 (en) |
DK (1) | DK107296C (en) |
GB (1) | GB1022031A (en) |
SE (1) | SE313820B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7534900B2 (en) * | 2005-03-14 | 2009-05-19 | Teva Pharmaceutical Industries Ltd | Process for the purification of duloxetine hydrochloride |
-
1963
- 1963-04-23 GB GB15974/63A patent/GB1022031A/en not_active Expired
- 1963-05-07 CS CS2617A patent/CS160625B2/cs unknown
- 1963-05-09 DK DK222363AA patent/DK107296C/en active
- 1963-05-10 SE SE5189/63A patent/SE313820B/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7534900B2 (en) * | 2005-03-14 | 2009-05-19 | Teva Pharmaceutical Industries Ltd | Process for the purification of duloxetine hydrochloride |
Also Published As
Publication number | Publication date |
---|---|
CS160625B2 (en) | 1975-03-28 |
DK107296C (en) | 1967-05-16 |
SE313820B (en) | 1969-08-25 |
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