Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43521Generated: October 28, 2026

Ethyl 1-(2-bromoacetyl)cyclopropanecarboxylate → Ethyl cis(+/-)-[2-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidin-1-yl)-1,3-thiazol-4-yl]cyclopropanecarboxylate

https://huagongshe.com/reaction/43521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-(2-bromoacetyl)cyclopropanecarboxylateHCID 11436266—
ReactantHCID 86648527HCID 86648527—
ProductEthyl cis(+/-)-[2-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidin-1-yl)-1,3-thiazol-4-yl]cyclopropanecarboxylateHCID 86648528—

Reaction Steps

The same operation as in Example (22b) was performed using cis(±)-N-(1-carbamothioyl-3-methoxypiperidin-4-yl)-4-chloro-5-ethyl-1H-imidazole-2-carboxamide obtained by the method described in Example (65c) (40 mg, 0.12 mmol) and ethyl 1-(bromoacetyl)cyclopropanecarboxylate obtained according to a method known in the literature (Heterocycles, 63, 3, 2004, 699-706) (60 mg, 0.26 mmol), to obtain 23.5 mg of the title compound as a colorless oily substance (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-8f5925430f50482e932ca7d4054bb707
Source noteuspto-grants-2013_09