Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250452Generated: October 26, 2026

Triethylamine → [(4-Benzyloxy-1-dimethylcarbamoyl-isoquinoline-3-carbonyl)-amino]-acetic acid benzyl ester

https://huagongshe.com/reaction/250452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBenzyl 2-aminoacetate hydrochlorideHCID 11701227—
Reactant4-Benzyloxy-1-dimethylcarbamoyl-isoquinoline-3-carboxylic acidHCID 66713108—
SolventDichloromethaneHCID 6344—
Product[(4-Benzyloxy-1-dimethylcarbamoyl-isoquinoline-3-carbonyl)-amino]-acetic acid benzyl esterHCID 66712806—

Reaction Steps

To a mixture of 4-benzyloxy-1-dimethylcarbamoyl-isoquinoline-3-carboxylic acid (210 mg, 0.6 mmol), NEt3 (175 μl, 1.25 mmol), and CH2Cl2 (12 ml) cooled with an ice bath was added ClCO2iBu (83 μl, 0.63 mmol) with stirring. After stirring for 15 min glycine benzyl ester hydrochloride (127 mg, 0.63 mmol) was added and the mixture was stirred for another 15 min before the ice bath was removed. Stirring was then continued at ambient temperature for additional 1.5 h. Subsequently; the mixture was concentrated in vacuo. To the residue was added water (10 ml) and a few drops of aqueous 6N HCl. The mixture was extracted with EtOAc (15 ml). The organic phase was dried over MgSO4 and concentrated in vacuo to give a yellowish gum. Purification by flash column chromatography on silica gel using hexanes:EtOAc=7:3 as the eluent gave the title compound as a slightly yellowish gum (211 mg); MS-(+)-ion: M+1=498.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863292B2
Source datasetuspto-grants-2011_01
ORD IDord-2e8887b2bf6c427f93c2b0732ead50e7
Source noteuspto-grants-2011_01