CN1189460C - New method of preparing Granisetron intermediate - Google Patents
New method of preparing Granisetron intermediate Download PDFInfo
- Publication number
- CN1189460C CN1189460C CN 03100765 CN03100765A CN1189460C CN 1189460 C CN1189460 C CN 1189460C CN 03100765 CN03100765 CN 03100765 CN 03100765 A CN03100765 A CN 03100765A CN 1189460 C CN1189460 C CN 1189460C
- Authority
- CN
- China
- Prior art keywords
- carboxylic acid
- preparing
- methylindazole
- methyl
- acetone
- 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 - Lifetime
Links
Landscapes
- Plural Heterocyclic Compounds (AREA)
Abstract
The present invention discloses a new method of preparing 1-methyl-3-carboxylic acid. The compound is an important intermediate for synthesizing 5-HT receptor inhibitors such as granisetron, etc. The present invention uses methylated reagents to methylate indazole-3-carboxylic acid in a water-bearing mixed solvent where alkali exists, is the simple, convenient, safe and effective method of preparing 1-methyl-3-carboxylic acid and is suitable for industrialization production on a large scale.
Description
Technical field
The invention discloses a kind of novel method of easy preparation 1-methylindazole-3-carboxylic acid (I).This compound is synthetic 5-HT acceptor inhibitor, as the important intermediate of granisetron (Granisetron) etc.
Background technology
Background technology of the present invention is as follows:
Usually, 1-methylindazole-3-carboxylic acid (I) can be formed (as US4 via methylating by indazole-3-carboxylic acid (II), 946,966 report), considering has two nitrogen-atoms to exist on the indazole ring, all might be methylated, the ordinary method products therefrom is the mixture of 1-methylindazole-3-carboxylic acid and 2-methylindazole-3-carboxylic acid, needs with the method for chromatography it to be separated.U.S. Pat 4,946 has been reported a kind of method that can optionally obtain 1-methylindazole-3-carboxylic acid for 966, is to adopt anhydrous polar solvent (as alcohols), and be that alkali methylates with the sodium alkoxide.When using this method, preparing sodium isopropylate with sodium Metal 99.5 and isopropanol reaction has certain danger, and needs the long period.In addition, in experimenting, we find out that, forms sodium salt behind sodium isopropylate and the raw material indazole-3-carboxylic acid reaction, be insoluble to the absolute alcohol kind solvent, cause methylation reaction incomplete, need to reclaim the intact raw material of unreacted, operate more loaded down with trivial detailsly, actual recovery is far below 85～90% yields of being reported.In addition, this method requires anhydrous system, protection of inert gas, and severe reaction conditions is unfavorable for large-scale industrialization production.
Purpose of the present invention, just provide a kind of easy, safe, prepare the method for 1-methylindazole-3-carboxylic acid (I) efficiently, be suitable for large-scale industrialization production.
Summary of the invention
Technical scheme of the present invention is as follows:
We find when synthesizing this compound, (volume ratio is 3: 1～10: 1 at polar solvent such as acetone and water, preferably 6: 1) mixed solvent in, or in the mixed solvent of rudimentary alcohol and water (as methyl alcohol, ethanol, propyl alcohol or Virahol and water, volume ratio is mixing in 3: 1～10: 1, preferred 5: 1～6: 1,) be alkali with alkali metal hydroxides such as sodium hydroxide or potassium hydroxide, with methyl-sulfate or methyl iodide etc. is methylating reagent, indazole-3-carboxylic acid (II) is carried out methylation reaction, can obtain the 1-methylindazole-3-carboxylic acid of higher degree, TLC detects and does not find raw material (II), illustrate that transformation efficiency is 100%, recrystallization can obtain pure 1-methylindazole-3-carboxylic acid.
Because the methyl iodide price is higher, takes all factors into consideration raw materials cost and product yield, preferred version of the present invention is: mixed solvent is acetone (volume ratio is 6: 1), and alkali is sodium hydroxide, and methylating reagent is a methyl-sulfate.
The method for preparing 1-methylindazole-3-carboxylic acid (I) of the present invention, compared with prior art, adopt the Aquo System of polar solvent, as acetone and water or lower alcohol/water, with alkali metal hydroxides such as industrial sodium hydroxide commonly used or potassium hydroxide is alkali, substitute sodium alkoxide/absolute alcohol, had cheapness, safety, advantages of simple operation; Reaction mixture is a unitary system, no insolubles, and raw material reaction is complete, and product yield is in pure product, and acetone and aqueous systems can reach more than 85%, and the system of lower alcohol/water can reach more than 70%; Reaction conditions does not have particular requirement, need not the no water treatment and the protection of inert gas of equipment and raw material, is suitable for large-scale industrialization production.
Embodiment
Embodiment 1:
In the 50L reactor, add 30L acetone, stir and drop into 3 kilograms of indazole-3-carboxylic acids (18.5mol) down, stir after 15 minutes, add the 4L methyl-sulfate, continue to stir half an hour, slowly add aqueous sodium hydroxide solution (the 5.6kg sodium hydroxide for preparing, 5 premium on currency), slowly be warming up to backflow, about 2 hours, the TLC detection reaction does not have raw material fully, normal pressure steams and removes about 15 liters of acetone, is cooled to room temperature, adds the dilution of 3 premium on currency, transfer PH to 1 with concentrated hydrochloric acid, the cooling suction filtration, drying gets 4.5kg crude product 1-methylindazole-3-carboxylic acid, with 50% aqueous ethanolic solution recrystallization, get 2.8 kilograms of pure 1-methylindazole-3-carboxylic acids, yield 85%, m.p.:215 ℃, mix with standard model (m.p.:215 ℃), fusing point does not descend.
This embodiment is a preferred version of the present invention.
Embodiment 2:
In the 10L reactor, add 3L 95% ethanol, stir and drop into 300 gram indazole-3-carboxylic acids (1.85mol) down, stir after 15 minutes, add 400 milliliters of methyl-sulfates, continue to stir half an hour, slowly add the aqueous sodium hydroxide solution (560g sodium hydroxide, 0.5 premium on currency) for preparing, slowly be warming up to backflow, about 1 hour, the TLC detection reaction is complete, and post-processing step gets 400g crude product 1-methylindazole-3-carboxylic acid with embodiment 1,50% aqueous ethanolic solution recrystallization, get the pure 1-methylindazole-3-carboxylic acid of 240g, yield 74%, m.p.:213 ℃.
Embodiment 3:
In the 5L reactor, add 3L acetone, stir down and drop into 200g indazole-3-carboxylic acid (1.2mol), stir after 15 minutes, add the 200g methyl iodide, continue to stir half an hour, slowly add the aqueous sodium hydroxide solution (380g sodium hydroxide, 0.5 premium on currency) for preparing, slowly be warming up to backflow, add the 100g methyl iodide after 3 hours, continue to reflux 2 hours, the TLC detection reaction is complete, normal pressure steams and removes about 1.5 liters of solvents, be cooled to room temperature, add the dilution of 2 premium on currency, transfer PH to 1 with concentrated hydrochloric acid, the cooling suction filtration, drying, 50% aqueous ethanolic solution recrystallization gets the pure 1-methylindazole-3-carboxylic acid of 198g, yield 91%, m.p.:216 ℃.
Claims (5)
1, a kind of method for preparing 1-methylindazole-3-carboxylic acid is characterized in that in volume ratio was 3: 1～10: 1 acetone, alkali metal hydroxide existed down, with methylating reagent indazole-3-carboxylic acid is methylated.
2, the method for preparing 1-methylindazole-3-carboxylic acid according to claim 1, the volume ratio that it is characterized in that acetone is 6: 1.
3, the method for preparing 1-methylindazole-3-carboxylic acid according to claim 1 is characterized in that alkali metal hydroxide is sodium hydroxide or potassium hydroxide.
4, the method for preparing 1-methylindazole-3-carboxylic acid according to claim 1 is characterized in that methylating reagent is methyl-sulfate or methyl iodide.
5, the method for preparing 1-methylindazole-3-carboxylic acid according to claim 1, the volume ratio of its feature acetone is 6: 1, and alkali is sodium hydroxide, and methylating reagent is a methyl-sulfate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 03100765 CN1189460C (en) | 2003-01-23 | 2003-01-23 | New method of preparing Granisetron intermediate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 03100765 CN1189460C (en) | 2003-01-23 | 2003-01-23 | New method of preparing Granisetron intermediate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1429816A CN1429816A (en) | 2003-07-16 |
| CN1189460C true CN1189460C (en) | 2005-02-16 |
Family
ID=4789888
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 03100765 Expired - Lifetime CN1189460C (en) | 2003-01-23 | 2003-01-23 | New method of preparing Granisetron intermediate |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1189460C (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103319396A (en) * | 2012-03-21 | 2013-09-25 | 黑龙江福和华星制药集团股份有限公司 | Method for preparing 1-methylindole-3-carboxylic acid |
| CN103497156A (en) * | 2013-09-18 | 2014-01-08 | 苏州岚云医药科技有限公司 | 1-N-substitution method of fused ring pyrazole compounds |
-
2003
- 2003-01-23 CN CN 03100765 patent/CN1189460C/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CN1429816A (en) | 2003-07-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN112250685B (en) | Preparation method of indolo [2,3-A ] carbazole | |
| CN112851544A (en) | Synthetic method of O- (3-chloro-2-propenyl) hydroxylamine | |
| CN103539662B (en) | Preparation and recovery method of 2-methyl-5-iodobenzoic acid | |
| CN103224451A (en) | Method for synthesizing 3,5-dichlorobenzoic acid | |
| CN1189460C (en) | New method of preparing Granisetron intermediate | |
| CN103242190B (en) | Synthetic method of propyzamide | |
| CN113683571A (en) | Preparation method of 2-methyl-5-bromopyrimidine | |
| CA2275253C (en) | Method for producing n-substituted 3-hydroxypyrazoles | |
| CN107188888A (en) | A kind of methanesulfonic acid for preparing steps the auspicious method for Buddhist nun | |
| CN109956884A (en) | A kind of preparation method of Phenylmethoxyamine hydrochloride | |
| CN108976122A (en) | The method for preparing 1,3- dicarbonyl compound based on metal hydride/palladium compound system | |
| CN105061232A (en) | Preparation method for red base B | |
| CN114349633A (en) | Process for the preparation of diesters of glutaconic acid | |
| CN108129531A (en) | A kind of preparation method of hesperidin methyl | |
| CN103772151A (en) | Preparation method of 2-methyl-3-phenyl benzyl alcohol | |
| CN103387595B (en) | A kind of preparation method of prednisolone | |
| CN108727167B (en) | Preparation method of anoplophora chinensis gathering pheromone | |
| CN102173993B (en) | Method for synthesizing 4,6-diamino resorcinol dihydrochloride (DAR) | |
| CN1207388A (en) | Process for producing 1-aminopyrrolidine, and 1-aminopyrrolidine according to the process | |
| CN106316950A (en) | Gliquidone preparation method | |
| CN112679378B (en) | Preparation method of oxadiazon intermediate 2,4-dichloro-5-isopropoxyphenylhydrazine | |
| CN103193767B (en) | The preparation method of the two benzene pyrrone-2-C-β-D-glucopyranoside of 1,6,7-trihydroxy--3-methoxyl group | |
| CN103508929B (en) | Synthetic method of 3-methylmercapto-diphenylamine | |
| CN113121317B (en) | Synthesis method of 1, 4-dichloro-2- (chloromethyl) -5-ethoxybenzene | |
| CN117986204B (en) | Synthesis method of dyclonine hydrochloride |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C56 | Change in the name or address of the patentee |
Owner name: NINGBO TEAM PHARMACEUTICAL CO., LTD. Free format text: FORMER NAME: NINGBO TIANHENG PHARMACEUTICAL FACTORY |
|
| CP01 | Change in the name or title of a patent holder |
Address after: 315201, No. three, No. 6, Zhen Zhuang Town, Zhenhai District, Zhejiang, Ningbo Patentee after: Ningbo Team Pharmaceutical Co.,Ltd. Address before: 315201, No. three, No. 6, Zhen Zhuang Town, Zhenhai District, Zhejiang, Ningbo Patentee before: Ningbo Tianheng Pharmaceutical Factory |
|
| C56 | Change in the name or address of the patentee |
Owner name: FU'AN PHARMACEUTICAL GROUP NINGBO TEAM PHARM CO., Free format text: FORMER NAME: NINGBO TEAM PHARMACEUTICAL CO., LTD. |
|
| CP01 | Change in the name or title of a patent holder |
Address after: 315201, No. three, No. 6, Zhen Zhuang Town, Zhenhai District, Zhejiang, Ningbo Patentee after: FUAN PHARMACEUTICAL GROUP NINGBO TEAM PHARMACEUTICAL CO.,LTD. Address before: 315201, No. three, No. 6, Zhen Zhuang Town, Zhenhai District, Zhejiang, Ningbo Patentee before: Ningbo Team Pharmaceutical Co.,Ltd. |
|
| CX01 | Expiry of patent term | ||
| CX01 | Expiry of patent term |
Granted publication date: 20050216 |