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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528832Generated: October 25, 2026

1-ethyl-2,3-dihydro-1H-indole-5-sulfonamide → 1-(3,4-Dichlorophenethyl)indoline-5-sulfonamide

https://huagongshe.com/reaction/528832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ethyl-2,3-dihydro-1H-indole-5-sulfonamideHCID 32103726—
Reactant1-(2-(3,4-Dichlorophenyl)acetyl)indoline-5-sulfonamideHCID 71061053—
Product1-(3,4-Dichlorophenethyl)indoline-5-sulfonamideHCID 7108618666%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 53, 1-(2-(3,4-dichlorophenyl)acetyl)indoline-5-sulfonamide (Intermediate 64, 140 mg, 0.363 mmol) was converted to the title compound (89 mg, 66%) after purification using preparative HPLC. 1H NMR (DMSO-d6) δ 7.64-7.63 (m, 1H), 7.54 (d, J=8.1 Hz, 1H), 7.43 (dd, J=8.4, 2.0 Hz, 1H), 7.39 (d, J=1.5 Hz, 1H), 7.33 (dd, J=8.3 Hz, 2.1 Hz, 1H), 6.90 (s, 2H), 6.56 (d, J=8.4 Hz, 1H), 3.49 (t, J=8.7 Hz, 2H), 3.42-3.38 (m, 2H), 2.95 (t, J=8.5 Hz, 2H), 2.84 (t, J=7.5 Hz, 2H); MS(ESI+) m/z 371.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-7eee0e02ed6c4cfd876211ac4c276c5f
Source noteuspto-grants-2016_05