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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190636Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → 4-[5-(4-Iodo-3-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2190636

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamideHCID 59318138—
Reactant4-[5-(3-Iodo-4-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 59318184—
Product4-[5-(4-Iodo-3-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 59318120—

Reaction Steps

4-[5-(4-Iodo-3-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl ester was prepared from 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide and 1-Boc-piperazine following a procedure similar to the one described in the synthesis of 4-[5-(3-iodo-4-methyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carboxylic acid tert-butyl ester above. The product was obtained after silica gel column purification with 20-40% EtOAc in hexanes gradient. HRMS m/z calcd for C22H27N4O3I [M+H]+: 523.1201. Found: 523.1202.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-57bba8ca401a4039bdabc7b2580bd9f3
Source noteuspto-grants-2012_12