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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733555Generated: November 1, 2026

Acetic Anhydride → HCID 20300066, compound

https://huagongshe.com/reaction/1733555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Pyridinecarboxylic acid, 2-((1-ethyl-2-methyl-1H-indol-3-yl)carbonyl)-HCID 112344—
Reactant6-(4-Methoxyphenyl)imidazo[2,1-b]thiazoleHCID 369507—
SolventWaterHCID 962—
ProductHCID 20300066HCID 20300066123.6%

Reaction Steps

A mixture of 0.92 gram of 6-p-methoxy phenylimidazo[2,1-b]thiazole, 0.69 gram of (1-ethyl-2-methylindol-3-yl)(3-carboxypyridin-2-yl)ketone and 20 ml. of acetic anhydride was stirred 2.5 hours at 50° C. The reaction solution was poured into 250 ml. of water and adjusted to pH 9.8 with ammonium hydroxide. After one hour stirring the solid material was filtered and washed with water to give 1.44 grams (95%) of desired product, mp. 115°-118° C. The infrared spectrum showed a strong 1770 cm-1 lactone carbonyl peak. A solution of the product on silica gel produced a purple color.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242513
Source datasetuspto-grants-1980_12
ORD IDord-4b1c835a998f463aafd6d4f2241a8553
Source noteuspto-grants-1980_12