Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448776Generated: October 26, 2026

Methyl 1-aminocyclohexanoate → 1-[[[4-[2-[4-(4-Morpholinyl)-1-piperazinyl]-4-thiazolyl]phenyl]carbonyl]amino]cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/448776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-aminocyclohexanoateHCID 4048819—
Reactant4-[2-[4-(4-Morpholinyl)-1-piperazinyl]-4-thiazolyl]benzoic acid hydrobromideHCID 67181771—
Product1-[[[4-[2-[4-(4-Morpholinyl)-1-piperazinyl]-4-thiazolyl]phenyl]carbonyl]amino]cyclohexanecarboxylic acid methyl esterHCID 67182490—

Reaction Steps

4.50 g (9.90 mmol) of 4-[2-[4-(4-morpholinyl)-1-piperazinyl]-4-thiazolyl]benzoic acid hydrobromide was used instead of 4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]benzoic acid hydrobromide, and 1.57 g (9.90 mmol) of 1-aminocyclohexanecarboxylic acid methyl ester was used instead of 1-aminocyclohexanecarboxylic acid phenylmethyl ester in the process according to Reference Example 210 to obtain 5.08 g (quantitative) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481725B2
Source datasetuspto-grants-2013_07
ORD IDord-fe988b498058463d9769fa9d6dd5c79a
Source noteuspto-grants-2013_07