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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891478Generated: November 2, 2026

Ethanesulfonylchloride, 2-chloro- → HCID 58367160, compound

https://huagongshe.com/reaction/1891478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
Reactant(S)-5-(5-(1-amino-2,3-dihydro-1H-inden-4-yl)-1,3,4-thiadiazol-2-yl)-2-isopropoxybenzonitrile hydrochlorideHCID 67193845—
SolventDichloromethaneHCID 6344—
ProductHCID 58367160HCID 5836716066%

Reaction Steps

To a stirred solution of (5)-5-(5-(1-amino-2,3-dihydro-1H-inden-4-yl)-1,3,4-thiadiazol-2-yl)-2-isopropoxybenzonitrile hydrochloride 4 (40 mg, 0.5 mmol) and TEA (49 mg, 0.48 mmol) in DCM (2 mL) was added 2-chloroethanesulfonyl chloride (79 mg, 0.48 mmol) at 0° C. The reaction was warmed to room temperature and stirred for 2 h. The reaction was quenched by the addition of NaHCO3. The product was purified by chromatography (EA/hexane) to provide 30 mg (66%) of (S)-N-(4-(5-(3-cyano-4-isopropoxyphenyl)-1,3,4-thiadiazol-2-yl)-2,3-dihydro-1H-inden-1-yl)ethenesulfonamide as yellow solid. LCMS-ESI (m/z) calculated for C23H22N4O3S2: 466.1; found 467.1 [M+H]+, tR=3.63 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507538B2
Source datasetuspto-grants-2013_08
ORD IDord-23aa10705fb148edb2f12847f76e0f45
Source noteuspto-grants-2013_08