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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190542Generated: November 3, 2026

4-[5-(4-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl ester → N-(4-tert-Butyl-phenyl)-6-piperazin-1-yl-nicotinamide

https://huagongshe.com/reaction/2190542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[5-(4-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 59318021—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(4-tert-Butyl-phenyl)-6-piperazin-1-yl-nicotinamideHCID 5931801958.4%

Reaction Steps

4-[5-(4-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl ester (200 mg, 0.45 mmol) was dissolved at rt in a mixture of 30% TFA in CH2Cl2. The reaction mixture was stirred until TLC indicated consumption of starting material (30 min). The mixture was then partitioned between EtOAc and water. The water layer was basified with solid NaOH to pH 12. The organic layer was separated and the aqueous layer was extracted again with EtOAc. The combined organic layer was washed with water, dried over Na2SO4, filtered and concentrated to afford the product (89 mg, Yield: 56%). HRMS m/z calcd for C20H26N4O [M+H]+: 339.2180. Found: 339.2180.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-9f2540f70ebb4677a193e44689c31c1f
Source noteuspto-grants-2012_12