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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58701Generated: October 29, 2026

Diisopropylethylamine → N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(4-isopropylphenyl)-2-oxopyrrolidine-3-carboxamide

https://huagongshe.com/reaction/58701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
Reactant2-Oxo-1-[4-(propan-2-yl)phenyl]pyrrolidine-3-carboxylic acidHCID 24275217—
SolventDimethylformamideHCID 6228—
ProductN-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(4-isopropylphenyl)-2-oxopyrrolidine-3-carboxamideHCID 6683195332.3%

Reaction Steps

A mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.036 g; 0.146 mmol), PyBOP (0.113 g; 0.219 mmol), N,N-diisopropylethylamine (0.075 mL; 0.437 mmol) and 1-(4-isopropylphenyl)-2-oxopyrrolidine-3-carboxylic acid (0.100 g; 0.425 mmol) was stirred in DMF (3 mL) overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulfate, the organic layer was washed with sodium carbonate, brine, dried and concentrated under reduced pressure. The crude mixture was purified flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.020 g (32%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434722B2
Source datasetuspto-grants-2016_09
ORD IDord-7dcccc8ca0584af586f74b00beaaa53a
Source noteuspto-grants-2016_09