Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395744Generated: October 29, 2026

Triethylamine → tert-Butyl 4-(6-chloro-5-nitropyrimidin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2395744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,6-Dichloro-5-nitropyrimidineHCID 20312—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Producttert-Butyl 4-(6-chloro-5-nitropyrimidin-4-yl)piperazine-1-carboxylateHCID 21477639—

Reaction Steps

A solution of 1-[1,1-dimethylethoxycarbonyl]piperazine (1.88 g) in dichloromethane (30 ml) is added drop by drop over 1.5 hr to a solution of 4,6-dichloro-5-nitropyrimidine (1.94 g) and triethylamine (1.32 g) in dichloromethane (170 ml) at - 78°. After stirring an additional hr at -78°, the reaction is diluted with aqueous sodium bicarbonate (10%). The phases are separated, the organic phase is concentrated to a liquid which solidified on standing at 20°-25°. The solid is dissolved in chloroform and flash chromatographed on silica gel eluting with methanol/chloroform (1/99), pooling and concentrating the appropriate fractions gives the title compound, Anal. Calc for C13H18N5ClO4 ; MW=343.77: C,45.42; H,5.28; N,20.37; Cl,10.31. Found: C,45.52; H,5.40; N,20.34; Cl,10.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489593
Source datasetuspto-grants-1996_02
ORD IDord-7ccbc13b279641a9947f2403c86b20cb
Source noteuspto-grants-1996_02