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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528824Generated: October 25, 2026

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

https://huagongshe.com/reaction/528824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ethyl-2,3-dihydro-1H-indole-5-sulfonamideHCID 32103726—
Reactant1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
Product1-(Cyclohexylmethyl)indoline-5-sulfonamideHCID 3491400557%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 53, 1-(cyclohexanecarbonyl)indoline-5-sulfonamide (Intermediate 55, 120 mg, 0.39 mmol) was converted to the title compound (65 mg, 57%) after purification using preparative HPLC. 1H NMR (CD3OD) δ 7.54 (dd, J=8.4, 2.0 Hz, 1H), 7.45 (d, J=1.5 Hz, 1H), 6.38 (d, J=8.4 Hz, 2H), 3.54 (d, J=8.7 Hz, 2H), 3.04-2.96 (m, 4H), 1.80-1.68 (m, 6H), 1.31-1.23 (m, 3H), 1.05-0.96 (m, 2H); MS(ESI+) m/z 295.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-30ed4f1a09c14cc186f1d1e457b53471
Source noteuspto-grants-2016_05