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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528829Generated: October 25, 2026

3,4-Difluorobenzoyl chloride → 1-(3,4-Difluorobenzoyl)indoline-5-sulfonamide

https://huagongshe.com/reaction/528829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Difluorobenzoyl chlorideHCID 2724519—
Reactant2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
Reactant1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
Product1-(3,4-Difluorobenzoyl)indoline-5-sulfonamideHCID 7108644078.8%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 90 mg, 0.45 mmol) and 3,4-difluorobenzoyl chloride (69 μL, 0.54 mmol) were converted to the title compound (120 mg, 78%). 1H NMR (DMSO-d6) δ 7.60-7.21 (m, 6H), 7.01 (s, 2H), 3.85 (t, J=8.6 Hz, 2H), 2.92 (t, J=8.6 Hz, 2H); MS(ESI+) m/z 338.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-c0045dcafec34760bf8796cbecb3c20c
Source noteuspto-grants-2016_05