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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979944Generated: October 27, 2026

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

https://huagongshe.com/reaction/1979944

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 numberUS04483859
Source datasetuspto-grants-1984_11
ORD IDord-b7a94321cbfc400694dc368fc88f9c81
Source noteuspto-grants-1984_11