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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271125Generated: October 26, 2026

Diisopropylcarbodiimide → 4-[4-[[(Phenylmethoxy)amino]carbonyl]phenyl]-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/1271125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
Reactant4-[4-(tert-Butoxycarbonyl)piperazin-1-yl]benzoic acidHCID 2795508—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-[4-[[(Phenylmethoxy)amino]carbonyl]phenyl]-1-piperazinecarboxylic acid, 1,1-dimethylethyl esterHCID 86598201104%

Reaction Steps

A mixture of 4-(4-carboxyphenyl)-1-piperazinecarboxylic acid, 1-(1,1-dimethylethyl) ester (0.032 mol), O-(phenylmethyl)-hydroxylamine hydrochloride (0.064 mol), DMAP (0.03 mol) in DCM p.a. (250 ml) and TEA (14 ml) was stirred at room temperature. DIC (0.064 mol) was added. The reaction mixture was stirred at room temperature for 8 hours, then washed with water, HCl (0.5N) and water. The separated organic layer was dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: DCM/MeOH 98/2). The desired fractions were collected and the solvent was evaporated, yielding 13.7 g of 4-[4-[[(phenylmethoxy)amino]carbonyl]phenyl]-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester (interm. 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205304B2
Source datasetuspto-grants-2007_04
ORD IDord-5e347170476e41eaa4ddd18dfc2abb1c
Source noteuspto-grants-2007_04