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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241405Generated: October 30, 2026

2-Bromo-N-cyclopropylacetamide → 2-(4-{6-[(5-Cyano-1,3-thiazol-2-yl)amino]pyrimidin-4-yl}piperazin-1-yl)-N-cyclopropyl-acetamide

https://huagongshe.com/reaction/1241405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-N-cyclopropylacetamideHCID 16757560—
Reactant2-(6-(Piperazin-1-yl)pyrimidin-4-ylamino)thiazole-5-carbonitrileHCID 21934630—
SolventChloroformHCID 6212—
Product2-(4-{6-[(5-Cyano-1,3-thiazol-2-yl)amino]pyrimidin-4-yl}piperazin-1-yl)-N-cyclopropyl-acetamideHCID 21934698—

Reaction Conditions

Temperature100 °C

Reaction Steps

12-3 (0.2 g, 0.39 mmol) and 2-bromo-N-cyclopropylacetamide 38-1 (0.069 g, 0.39 mmol) were suspended in chloroform/2M Na2CO3 in a sealed tube and heated in a Smith Personal Chemistry microwave reactor at 100° C. for 20 minutes. The solid was then filtered off and purified on a silica column to afford 38-2. Hi-Res MS: calc: 385.1554 found: 385.1548. 1H-NMR (CD3OD): 8.39(s, 1H); 7.99(s, 1H); 6.14(s, 1H); 3.68(m, 4H); 3.05(s, 2H); 2.70(m, 1H); 2.58(m, 4H); 0.75(m, 2H); 0.55(m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115597B2
Source datasetuspto-grants-2006_10
ORD IDord-5016891323dc491ca8501aece2c21615
Source noteuspto-grants-2006_10