Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745003Generated: October 30, 2026

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

https://huagongshe.com/reaction/745003

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 numberUS05559246
Source datasetuspto-grants-1996_09
ORD IDord-23b3d01c411d440db14e637c7680a5c2
Source noteuspto-grants-1996_09