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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309651Generated: November 3, 2026

Acetic Anhydride → HCID 14013068, compound

https://huagongshe.com/reaction/2309651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 14013289HCID 14013289—
SolventWaterHCID 962—
ProductHCID 14013068HCID 1401306872%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4 parts of 2-amino-N-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]methyl]-1-piperidinyl]ethyl]benzamide, 20 parts of acetic acid anhydride and 40 parts of water was stirred and heated overnight at 120° C. After cooling, ice water was added. The whole was treated with ammonium hydroxide. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was converted into the (E)-2-butenedioate salt in ethanol. The salt was filtered off and dried, yielding 3.7 parts (72%) of 3-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]methyl]-1-piperidinyl]ethyl]-2-methyl-4(3H)-quinazolinone (E)-2-butenedioate (1:1); mp. 210.3° C. (481).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695575
Source datasetuspto-grants-1987_09
ORD IDord-8960c16fb8ca480bafbec3b740a59190
Source noteuspto-grants-1987_09