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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393253Generated: October 31, 2026

Pyrrole-2-Carboxylic Acid → (Pyrrole-2-carbonyl)-N-(benzyl)glycine-t-butyl ester

https://huagongshe.com/reaction/2393253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-Carboxylic AcidHCID 12473—
ReactantDiisopropylethylamineHCID 81531—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
ReactantTert-butyl 2-(benzylamino)acetateHCID 11020442—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(Pyrrole-2-carbonyl)-N-(benzyl)glycine-t-butyl esterHCID 7002010834.4%

Reaction Steps

To a suspension containing 3.00 g (27.0 mmol) of pyrrole-2-carboxylic acid in 75 mL of anhydrous dichloromethane under a nitrogen atmosphere at 0° C. was added 6.96 g (27.0 mmol of BOPCl and 14.1 mL (81.0 mmol) of DIEA. After stirring for 30 minutes, 5.97 g (27.0 mmol) of N-(benzyl)glycine-t-butyl ester was added and the reaction allowed to warn to room temperature overnight. The reaction was diluted with ethyl acetate and washed with a 5% potassium hydrogensulfate, saturated sodium bicarbonate solution and brine. The organic phase was dried over magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a gradient of 100% hexane to (60% hexane/ethyl acetate to afford 2.92 g (34.4%) of the title compound is a white solid. FAB MS [M+H] m/z Calcd: 315, Found: 315.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807829
Source datasetuspto-grants-1998_09
ORD IDord-f24f45aefd914f6b915b5d51f5cbe266
Source noteuspto-grants-1998_09