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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505721Generated: October 30, 2026

Chlorosulfamic acid → 6-phenethyl-7-(trifluoromethyl)-3,4-dihydro-[1,4]diazepino[6,7,1-hi]indole-2(1H)-sulfonamide

https://huagongshe.com/reaction/1505721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfamic acidHCID 24499—
ReactantN,N-DiethylethylenediamineHCID 60993—
Reactant6-Phenethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indoleHCID 86691988—
SolventDichloromethaneHCID 6344—
Product6-phenethyl-7-(trifluoromethyl)-3,4-dihydro-[1,4]diazepino[6,7,1-hi]indole-2(1H)-sulfonamideHCID 8669198931.5%

Reaction Steps

To a solution of 6-phenethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indole (93 mg, 0.24 mmol) in dichloromethane (3 mL) was added diethylaminoethyl amine (0.13 mL, 0.73 mmol) and sulfamoyl chloride (42 mg, 0.37 mmol). After stirring overnight, another portion of sulfamoyl chloride (42 mg) was added at 0° C., and the resulting mixture stirred for 2 h at room temperature. The resulting mixture was then concentrated under reduced pressure, and the residue was purified by reverse-phase chromatography (gradient 42%→90% TFA-H2O:acetonitrile) to yield 6-phenethyl-7-(trifluoromethyl)-3,4-dihydro-[1,4]diazepino[6,7,1-hi]indole-2(1H)-sulfonamide (32 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216998B2
Source datasetuspto-grants-2015_12
ORD IDord-29ee660238c244e79204fb42c13881e0
Source noteuspto-grants-2015_12