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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437448Generated: October 29, 2026

Acetic Acid → HCID 12535871, compound

https://huagongshe.com/reaction/437448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 12535828HCID 12535828—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 12535871HCID 1253587129%

Reaction Steps

A solution (1.9 ml.) of 37% formaldehyde (23.8 mmoles) in water followed by sodium cyanoborohydride (450 mg., 7.15 mmoles) were added to a stirred solution of ethyl 1,6-dihydro-6-oxo-2-(5-amino-2-ethoxyphenyl)pyrimidine-5-carboxylate (720 mg., 2.38 mmoles) in acetonitrile (14 ml.). Glacial acetic acid (0.24 ml.) was then added over a period of one minute. The mixture was stirred at room temperature for 2 hours. Additional glacial acetic acid (0.24 ml.) was added and stirring was continued for an extra 0.5 hour. The mixture was treated with diethyl ether (35 ml.). The organic layer was washed with 10% aqueous sodium bicarbonate (3 × 10 ml.) followed by brine (30 ml.) and dried (sodium sulfate). The solvent was removed and a solution of the residue in acetonitrile-diethyl ether was extracted with 1 N sodium hydroxide (3 × 20 ml.). The aqueous extract was acidified with glacial acetic acid to pH 6. The precipitate was collected and recrystallized from acetonitrile to give the title compound (210 mg., 29%), m.p. 187°-196°. Recrystallization from benzene-Skellysolve B gave analytical material, m.p. 195°-198°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031093
Source datasetuspto-grants-1977_06
ORD IDord-93daea7cb90042509499ed503232ab5e
Source noteuspto-grants-1977_06