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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077858Generated: November 3, 2026

Phosgene → 5-sulfonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole

https://huagongshe.com/reaction/1077858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
Reactant(R)-5-Amino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indoleHCID 10376533—
SolventAcetonitrileHCID 6342—
Product5-sulfonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indoleHCID 19970255—
Product5-carbonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indoleHCID 86749715—

Reaction Steps

To a stirred solution of (R)-5-amino-3-(N-methylpyrrolidin-2-ylmethyl) indole (0. 229 g, 1.00 mmol) and triethylamine (0.21 mL, 1.5 mmol, 1.5 eq) in anhydrous acetonitrile (3 mL) at 0° C. under nitrogen was added the appropriate carbonyl chloride or sulfonyl chloride (1.5 mmol, 1.5 eq). The resulting reaction mixture was stirred at room temperature for 12 hours. The reaction mixture was then evaporated under reduced pressure, and the residue was column chromatographed using silica gel (approximately 25 g) and elution with an appropriate solvent system afforded the appropriate 5-carbonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole or 5-sulfonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545644
Source datasetuspto-grants-1996_08
ORD IDord-bef4d8a6693e41d5981cf7cbacc216ad
Source noteuspto-grants-1996_08