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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602173Generated: October 30, 2026

1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acid → 1-(tert-Butoxycarbonyl)-N-[2-(4-chlorophenyl)-4-methylthiazol-5-yl]piperidine-3-carboxamide

https://huagongshe.com/reaction/602173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
Reactant5-Amino-2-(4-chlorophenyl)-4-methylthiazoleHCID 67267329—
Product1-(tert-Butoxycarbonyl)-N-[2-(4-chlorophenyl)-4-methylthiazol-5-yl]piperidine-3-carboxamideHCID 5899260830.1%

Reaction Steps

Using 5-amino-2-(4-chlorophenyl)-4-methylthiazole (197 mg, 0.877 mmol) and 1-(tert-butoxycarbonyl)nipecotic acid (205 mg, 0.877 mmol), the same procedure was followed as in Step 3a of Example 3 to give 115 mg (30%) of the desired compound as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-d329f90d64b24054b4c93333eed29394
Source noteuspto-grants-2011_03