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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395749Generated: October 28, 2026

Acetic Acid → 1,1-Dimethylethyl 4-[5-[(1-methylethyl)amino]-4-pyrimidinyl]-1-piperazinecarboxylate

https://huagongshe.com/reaction/2395749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 21477601HCID 21477601—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product1,1-Dimethylethyl 4-[5-[(1-methylethyl)amino]-4-pyrimidinyl]-1-piperazinecarboxylateHCID 21477621—

Reaction Steps

A solution of sodium cyanoborohydride (0.13 g) in methanol (4 ml) is added to a mixture of 1-[1,1-dimethylethoxycarbonyl]-4-[5-amino-6-pyrimidinyl]piperazine (PREPARATION 28, 0.44 g), acetone (3 ml), and glacial acetic acid (0.4 ml) in methanol (7 ml) at 0°. The mixture is stirred at 20°-25° for 72 h. The reaction is diluted with an aqueous sodium hydroxide solution (10%) and dichloromethane. The phases are separated and the organic phase is washed with water and the concentrated to a colorless liquid which is flash chromatographed on silica gel eluting with methanol/chloroform (1/99). The appropriate fractions are pooled and concentrated to give the title compound, NMR (CDCl3) 1.26, 1.49, 3.2, 3.44, 3.5-3.62, 7.89 and 8.33 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489593
Source datasetuspto-grants-1996_02
ORD IDord-5dd3477bfdc243668ddd08d353ca4a6c
Source noteuspto-grants-1996_02