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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70775Generated: October 26, 2026

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

https://huagongshe.com/reaction/70775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
Reactanttert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-3-methyl-butyl]carbamateHCID 86695593—
Producttert-butyl N-[[1-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]cyclopentyl]methyl]carbamateHCID 86695607—

Reaction Steps

tert-butyl N-[[1-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]cyclopentyl]methyl]carbamate was synthesized using 5-bromo-2,4-dichloro-pyrimidine and Intermediate L using analogous reaction conditions as described for tert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-3-methyl-butyl]carbamate. 1H NMR (600 MHz, DMSO-d) δ ppm 1.34 (s, 9H) 1.50-1.58 (m, 2H) 1.63-1.78 (m, 4H) 1.96-2.06 (m, 2H) 3.25 (d, J=6.15 Hz, 2H) 6.71 (s, 1H) 7.18 (t, J=6.29 Hz, 1H) 8.20 (s, 1H). LCMS (ESI) 405 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822683B2
Source datasetuspto-grants-2014_09
ORD IDord-ab5d221e05ac4b3eb00cb52eef78d286
Source noteuspto-grants-2014_09