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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588748Generated: October 25, 2026

Diisopropylethylamine → 2-Amino-4-[4-(tert-butoxycarbonyl)piperazin-1-yl]-6-chloropyrimidine-5-carboxaldehyde

https://huagongshe.com/reaction/588748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Amino-4,6-dichloropyrimidine-5-carboxaldehydeHCID 265546—
SolventDimethylformamideHCID 6228—
Product2-Amino-4-[4-(tert-butoxycarbonyl)piperazin-1-yl]-6-chloropyrimidine-5-carboxaldehydeHCID 89407451—

Reaction Steps

To a suspension of 2-amino-4,6-dichloropyrimidine-5-carboxaldehyde (3.84 g, 20 mmol) and DIPEA (5.2 mL, 30 mmol) in DMF was added tert-butyl piperazine-1-carboxylate (3.73 g, 20 mmol) portionwise. The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated and the residue obtained was precipitated with H2O. The precipitate was collected, washed with water and dried in vacuo, to provide the title compound as a white solid in quantitative yield. MS (m/z) 342 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227984B2
Source datasetuspto-grants-2016_01
ORD IDord-92767fc64e594fd0889bf904dbe89207
Source noteuspto-grants-2016_01