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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68550Generated: October 29, 2026

Triethylamine → Tert-butyl 4-(6-methoxypyrimidin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/68550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4-Chloro-6-methoxypyrimidineHCID 1051509—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(6-methoxypyrimidin-4-yl)piperazine-1-carboxylateHCID 66569709—

Reaction Conditions

Temperature60 °C

Reaction Steps

18.6 mL triethylamine and piperazine-1-carboxylic acid tert-butyl ester were added to 9.7 g 4-chloro-6-methoxy-pyrimidine in 50 mL DMF. The reaction was stirred over night at 60° C. The reaction was cooled and the precipitate was filtered. The filtrate was evaporated. The residue was dissolved in DCM, extracted with water and washed with sodium chloride solution. The solvent was evaporated and the residue was crystallized with a mixture of petrolether and diethylether (8:2) to yield 8.7 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822464B2
Source datasetuspto-grants-2014_09
ORD IDord-480b9947a2fb41b6ab3655deb9dd0a1b
Source noteuspto-grants-2014_09