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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437666Generated: October 30, 2026

Acetic Anhydride → HCID 21428838, compound

https://huagongshe.com/reaction/437666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 21428956HCID 21428956—
SolventWaterHCID 962—
ProductHCID 21428838HCID 21428838—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 9 parts of 2-amino-4-fluoro-N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro [4,5]dec-8-yl]ethyl}-benzamide, 8.5 parts of acetic acid anhydride and 85 parts of water is stirred for 30 minutes in a water-bath at about 80° C. The reaction mixture is cooled and alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The aqueous phase is separated and extracted with trichloromethane. The combined organic phases are washed three times with water, dried, filtered and evaporated. The residue is crystallized from 2-propanol. The product is filtered off and dried, yielding 5.2 parts of 2-(acetylamino)-4-fluoro-N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro-[4,5]dec-8-yl]ethyl}benzamide; mp. 195.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-9c012fbcba10462e81db522f563a513b
Source noteuspto-grants-1977_06