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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979930Generated: October 31, 2026

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

https://huagongshe.com/reaction/1979930

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 numberUS04483857
Source datasetuspto-grants-1984_11
ORD IDord-acdb1b01fa844875989d86d08f6a5c26
Source noteuspto-grants-1984_11