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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Benzyl 2-aminoacetate hydrochloride | HCID 11701227 | — |
| Reactant | 4-Benzyloxy-1-dimethylcarbamoyl-isoquinoline-3-carboxylic acid | HCID 66713108 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(4-Benzyloxy-1-dimethylcarbamoyl-isoquinoline-3-carbonyl)-amino]-acetic acid benzyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07863292B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-2e8887b2bf6c427f93c2b0732ead50e7 |
|---|
| Source note | uspto-grants-2011_01 |
|---|