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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708948Generated: November 1, 2026

2-(4-methoxyphenyl)-4-methyl-1,3-thiazole-5-carboxylic Acid → HCID 178488950, compound

https://huagongshe.com/reaction/1708948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-methoxyphenyl)-4-methyl-1,3-thiazole-5-carboxylic AcidHCID 4962843—
ReactantHCID 178509299HCID 178509299—
SolventDimethylformamideHCID 6228—
ProductHCID 178488950HCID 17848895064.4%

Reaction Steps

A solution of 300 mg (1.20 mmol) of 2-(4-methoxyphenyl)-4-methyl-5-thiazolecarboxylic acid and 292.7 mg (1.81 mmol) of N,N'-carbonyldiimidazole (CDI) in dry dimethylformamide (8 ml) was stirred at room temperature for 1 hour. Under the same conditions, a solution of 5-aminotetrazole (122.8 mg, 1.44 mmol) in dry dimethylformamide (1 ml) was added thereto and allowed to react at 70° C. for 3 hours. After the solvent was distilled off from the reaction mixture, the residue was treated with water under ice-cooling and acidified with 2N-HCl to pH 2. The produced solids were filtered with suction, suspended in 100 ml of water and made alkaline with 1N potassium hydroxide (pH=11). After the impurities were removed from the alkaline solution by extracting with ethyl acetate, the aqueous phase was acidified with 2N-HCl to pH 2 and the deposited solids were filtered with suction, washed with water and recrystallized from methanol-THF-water to give 244.4 mg (yield 64 %) of 2-(4-methoxyphenyl)-4-methyl-N-(1H-tetrazole-5-yl)-5-thiazolecarboxamide as white crystals, m.p. 275°-278° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946855
Source datasetuspto-grants-1990_08
ORD IDord-ee992df448cd4136963e668c668097cf
Source noteuspto-grants-1990_08