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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978453Generated: November 2, 2026

Acetic Anhydride → HCID 13851189, compound

https://huagongshe.com/reaction/978453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13851173HCID 13851173—
SolventAcetic AcidHCID 176—
ProductHCID 13851189HCID 13851189100%

Reaction Steps

A mixture of 5.8 parts of 7-amino-3-[4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl]-2,4(1H,3H)-quinazolinedione, 100 parts of acetic acid and 2.5 parts of acetic acid anhydride was stirred at reflux temperature. The reaction mixture was evaporated. The residue was stirred in water and ammonium hydroxide. The product was filtered off, washed with water and boiled in ethanol. After cooling, the product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 6.3 parts (100%) of N-[3-[4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl]-1,2,3,4-tetrahydro-2,4-dioxo-7-quinazolinyl]-acetamide; mp. 273.1° C. (18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665075
Source datasetuspto-grants-1987_05
ORD IDord-08561e07173949c49060e62b4fda5fe9
Source noteuspto-grants-1987_05