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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775306Generated: October 26, 2026

5-Bromo-2,4-dichloropyrimidine → benzyl N-[1-[[(5-bromo-2-chloro-pyrimidin-4-yl)amino]methyl]propyl]carbamate

https://huagongshe.com/reaction/1775306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
Reactant2-N-Cbz-butane-1,2-diamineHCID 45072685—
Reactanttert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]ethyl]carbamateHCID 86695590—
Productbenzyl N-[1-[[(5-bromo-2-chloro-pyrimidin-4-yl)amino]methyl]propyl]carbamateHCID 89825160—

Reaction Steps

benzyl N-[1-[[(5-bromo-2-chloro-pyrimidin-4-yl)amino]methyl]propyl]carbamate is synthesized by treating 5-Bromo-2,4-dichloropyrimidine with benzyl N-[1-(aminomethyl)propyl]carbamate using similar experimental conditions as described for the synthesis of tert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]ethyl]carbamate. LCMS (ESI) (M+H) 413

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260442B2
Source datasetuspto-grants-2016_02
ORD IDord-471c191ae4254fd59fecf3c296115a0f
Source noteuspto-grants-2016_02