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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065022Generated: October 25, 2026

Nitrogen → 4-[4-(2-Chloro-benzyloxycarbonylamino)-pyrazol-1-ylmethyl]-thiazole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2065022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chlorobenzyl chloroformateHCID 4072342—
Reactant4-(4-Amino-pyrazol-1-ylmethyl)-thiazole-2-carboxylic acid ethyl esterHCID 66928556—
SolventDichloromethaneHCID 6344—
Product4-[4-(2-Chloro-benzyloxycarbonylamino)-pyrazol-1-ylmethyl]-thiazole-2-carboxylic acid ethyl esterHCID 66928889—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-(4-amino-pyrazol-1-ylmethyl)-thiazole-2-carboxylic acid ethyl ester (1.43 g, 5.65 mmol) in CH2Cl2 (56.0 mL) was treated with DIPEA (1.15 mL, 8.47 mmol) followed by 2-chlorobenzylchloroformate (1.04 mL, 6.78 mmol). The reaction mixture was stirred at rt for 1 h before being quenched with water (50 mL), extracted with CH2Cl2 (3×40 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (96:4 CH2Cl2-MeOH) gave the title compound as a pink foam. TLC: rf (96:4 CH2Cl2-MeOH)=0.28. LC-MS-conditions 02: tR=0.99 min; [M+H]+=421.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-9066651e68a945f1a5ac0be5658afc38
Source noteuspto-grants-2012_10