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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602298Generated: October 29, 2026

Hydrochloric Acid → 4-Pyrimidinemethanol, 2-amino-

https://huagongshe.com/reaction/602298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 2-aminopyrimidine-4-carboxylateHCID 57971148—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product4-Pyrimidinemethanol, 2-amino-HCID 20049373%

Reaction Steps

2-Amino-4-methoxycarbonylpyrimidine (3.0 g, 20 mmol, Reference Compound No. 3-1) was suspended in a mixture solvent of ethanol (150 mL) and dichloromethane (20 mL), then sodium borohydride (2.2 g, 59 mmol) was added thereto at room temperature, and the whole was stirred for 24 hours. Acetone (20 mL) was added gradually under ice-cooling, and then 2M hydrochloric acid was added until the bubbles were no longer formed. Saturated aqueous sodium hydrogencarbonate solution was added to adjust the pH of the reaction mixture to 8, and the precipitated solid was filtered out. The filtrate was concentrated under reduced pressure, then suspended in a 10% methanol-chloroform solution, and the mixture was filtered again with silica gel (5.0 g). The filtrate was evaporated under reduced pressure, the precipitated solid was filtered off with ethyl acetate, and dried under reduced pressure to give 1.8 g of the title Reference Compound as a pale yellow solid (Yield: 73%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906511B2
Source datasetuspto-grants-2011_03
ORD IDord-1eff8aa604f84a80b31f972bf47ab66b
Source noteuspto-grants-2011_03