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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903085Generated: October 30, 2026

Triethylamine → 2-Chloro-4-(4-formylpiperazino)pyrimidine

https://huagongshe.com/reaction/1903085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant1-PiperazinecarboxaldehydeHCID 82191—
SolventEthanolHCID 702—
Product2-Chloro-4-(4-formylpiperazino)pyrimidineHCID 1386957031.5%

Reaction Steps

1-Formylpiperazine (38.5 g) and triethylamine (34 g) in ethanol (500 ml) were added slowly to a stirred solution of 2,4-dichloropyrimidine (50 g) in ethanol (2.5 ml) at room temperature. The mixture was stirred at room temperature for 24 hours then evaporated in vacuo and the residue partitioned between chloroform and water. The organic phase was washed with water and the combined aqueous phases extracted with chloroform. The combined chloroform extracts were dried (Na2SO4), evaporated in vacuo and the residue was crystallized twice from ethyl acetate to give 2-chloro-4-(4-formylpiperazino)pyrimidine, (24 g), m.p. 125°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435401
Source datasetuspto-grants-1984_03
ORD IDord-6bc1f37c7a844828b6f8a473bb1be76d
Source noteuspto-grants-1984_03