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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273970Generated: November 2, 2026

HCID 178464640, compound → HCID 178464641, compound

https://huagongshe.com/reaction/2273970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178464640HCID 178464640—
SolventTolueneHCID 1140—
ProductHCID 178464641HCID 17846464150.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

0.14 g 2,3-Dihydro-1H-indole-6-sulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide was dissolved in 25 mL toluene, the mixture was degassed, and 10 mol % of palladium on carbon was added. The mixture was stirred overnight at 50° C. The mixture was cooled to room temperature and filtered over Hyflo, and the Hyflo was washed with toluene. The filtrate was evaporated to dryness and the residue was purified by flash chromatography (DCM→DCM/EA 95:5→DCM/EA 8:2) to give 70 mg of 1H-Indole-6-sulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide as a white amorphous solid. 1H NMR (400 MHz, CDCl3) δ 0.86 (t, J=7.52 Hz, 3H), 1.06 (t, J=7.22 Hz, 3H), 1.32-1.57 (m, 2H), 2.89-3.00 (m, 1H), 3.35-3.54 (m, 3H), 3.89 (t, J=11.44 Hz, 1H), 6.54 (br.s., 1H), 6.84 (d, J=1.50 Hz, 1H), 6.96 (br.s., 1H), 7.36 (t, J=2.86 Hz, 1H), 7.59-7.70 (m, 2H), 8.26 (d, J=1.20 Hz, 1H), 9.55 (br.s., 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126942B2
Source datasetuspto-grants-2015_09
ORD IDord-9a2d788ef345409c9e98d870fc553dd1
Source noteuspto-grants-2015_09