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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528828Generated: October 26, 2026

Benzoyl chloride → 1-Benzoylindoline-5-sulfonamide

https://huagongshe.com/reaction/528828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
Reactant1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
Product1-Benzoylindoline-5-sulfonamideHCID 1768113779%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 100 mg, 0.50 mmol) and benzoyl chloride (64 μL, 0.56 mmol) were converted to the title compound (120 mg, 79%). 1H NMR (DMSO-d6) δ 7.70 (s, 1H), 7.65-7.60 (m, 3H), 7.57-7.49 (m, 4H), 7.24 (s, 2H), 4.07 (t, J=8.5 Hz, 2H), 3.15 (t, J=8.4 Hz, 2H); MS(ESI+) m/z 303.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-e980f2a76d114151a079ad587acb17b1
Source noteuspto-grants-2016_05