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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379857Generated: October 31, 2026

HCID 18368154, compound → HCID 18367865, compound

https://huagongshe.com/reaction/379857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18368154HCID 18368154—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 18367865HCID 1836786551.7%

Reaction Steps

3-Acetylamino-2-benzoyl-6-nitroindole (Example 152, 180 mg. 0.56 mmol) was hydrogenolyzed in the presence of palladium on activated carbon (5%, 18 mg) in ethanol (30 ml) at atmospheric pressure for 4 h. Catalyst was removed by filtration and the filtrate was concentrated. The residue was purified by flash column chromatography eluting with 0 to 50% ethyl acetate in hexanes and the product recrystallized from a mixture of methanol/ethyl acetate/hexane to give 85 mg of the title compound. m.p.: 219-221° C. 1H-NMR (DMSO-d6) δ: 10.9 (1H, br s), 9.54 (1H, s), 7.44-7.66 (5H, m), 7.38(1H, d, J=9.2 Hz), 6.47-6.45 (2H, m), 5.35 (2H, s), 1.69 (3H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300363B1
Source datasetuspto-grants-2001_10
ORD IDord-e0eb65e4ac1f4910b21c5dd1f16e75c5
Source noteuspto-grants-2001_10