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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918689Generated: October 25, 2026

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

https://huagongshe.com/reaction/1918689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyBOPHCID 2724699—
Reactant5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
Reactant1-(4-Methoxyphenyl)-2-oxo-3-pyrrolidinecarboxylic acidHCID 3373117—
SolventDimethylformamideHCID 6228—
ProductN-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(4-methoxyphenyl)-2-oxopyrrolidine-3-carboxamideHCID 6683200842.3%

Reaction Steps

A mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.098 g; 0.425 mmol), PyBOP (0.332 g; 0.638 mmol), N,N-diisoprpylethylamine (0.220 mL; 1.28 mmol) and 1-(4-methoxyphenyl)-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 0.074 g (42%) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-b8c48cae8101455e97de7d878ab507a2
Source noteuspto-grants-2013_12