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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528841Generated: October 26, 2026

Chloroacetyl chloride → 1-(2-chloroacetyl)-2,3-dihydro-1H-indole-5-sulfonamide

https://huagongshe.com/reaction/528841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
Reactant1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
Product1-(2-chloroacetyl)-2,3-dihydro-1H-indole-5-sulfonamideHCID 1622706123%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 500 mg, 2.52 mmol) and 2-chloroacetyl chloride (221 μL, 2.77 mmol) were converted to the title compound (160 mg, 23%). 1H NMR (DMSO-d6) δ 8.13 (d, J=8.1 Hz, 1H), 7.68-7.66 (m, 2H), 7.24 (s, 2H), 4.58 (s, 2H), 4.20 (t, J=8.5 Hz, 2H), 3.24 (t, J=8.5 Hz, 2H); MS(ESI+) m/z 275.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-6f495f5cca954443b21bb745420de5aa
Source noteuspto-grants-2016_05