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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528834Generated: October 25, 2026

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

https://huagongshe.com/reaction/528834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ethyl-2,3-dihydro-1H-indole-5-sulfonamideHCID 32103726—
Reactant1-(2-(Phenylthio)acetyl)indoline-5-sulfonamideHCID 71060712—
Product1-(2-(Phenylthio)ethyl)indoline-5-sulfonamideHCID 7106298557%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 53, 1-(2-(phenylthio)acetyl)indoline-5-sulfonamide (Intermediate 66, 74 mg, 0.21 mmol) was converted to the title compound (40 mg, 52%) after purification using preparative HPLC. 1H NMR (DMSO-d6) δ 7.43-7.33 (m, 6H), 7.21 (t, J=7.2. Hz, 1H), 6.90 (s, 2H), 6.36 (d, J=8.4 Hz, 1H), 3.53 (t, J=8.6 Hz, 2H), 3.39 (t, J=6.8 Hz, 2H), 3.19 (t, J=6.9 Hz, 2H), 2.94 (t, J=8.6 Hz, 2H); MS(ESI+) m/z 335.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-9cb86ddd57574206b32e148a9581c2e2
Source noteuspto-grants-2016_05