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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052505Generated: November 2, 2026

Benzyloxycarbonylglycine → HCID 131736174, compound

https://huagongshe.com/reaction/1052505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonylglycineHCID 14349—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 70979311HCID 70979311—
SolventEthyl AcetateHCID 8857—
ProductHCID 131736174HCID 13173617492.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

DIEA (10.5 ml, 60 mmol) was added at 0° C. over a mixture of 1-amino-3-bromo-N-phenyl-1H-pyrrole-2-carboxamide (5.1 g, 18 mmol) and 2-(benzyloxycabonylamino)acetic acid (5.33 g, 25 mmol) in anhydrous ethyl acetate (100 ml). After 15 min T3P® solution (50% AcOEt, 15 ml) was slowly added and stirred 20 min at 0° C. and then at room temperature overnight. Further DIEA (5 ml, 30 mmol), 2-(benzyloxycabonylamino)acetic acid (2.66 g, 25 mmol) and T3P® solution (50% AcOEt, 7 ml) were added and the reaction mixture was stirred at room temperature overnight. More ethyl acetate was added and the reaction crude was washed with water and brine, dried over magnesium sulphate and the solvent was removed under vacuum. The residue was purified by flash chromatography using Isolera® Purification System (0-40%, hexane-AcOEt) to give 7.81 g (41% yield) of the final product with a purity of 45% that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388189B2
Source datasetuspto-grants-2016_07
ORD IDord-29a4e3914499492096d83fc6ec8fa133
Source noteuspto-grants-2016_07