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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248244Generated: November 1, 2026

Formic Acid → HCID 86738423, compound

https://huagongshe.com/reaction/1248244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantHCID 20278959HCID 20278959—
ProductHCID 86738423HCID 8673842354%

Reaction Steps

A mixture of 7 parts of 2-amino-N-[3-[4-(4-fluorobenzoyl)-1-piperidinyl]propyl]benzamide, 12 parts of formic acid and 135 parts of methylbenzene is stirred and refluxed for 1 hour. Stirring at reflux is continued for 1 hour using a water-separator. The solvent is evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is converted into the (E)-2-butenedioate salt is 2-propanol. The salt is filtered off and dried, yielding 5 parts (54%) of 3-[3-[4-(4-fluorobenzoyl)-1-piperidinyl]propyl]-4(3H)-quinazolinone (E)-2-butenedioate (1:1); mp. 201.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522945
Source datasetuspto-grants-1985_06
ORD IDord-39e93908b1bc4bd9b530884a1d359b71
Source noteuspto-grants-1985_06