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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485753Generated: October 31, 2026

HCID 178482203, compound → HCID 178482196, compound

https://huagongshe.com/reaction/485753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178482203HCID 178482203—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178482196HCID 178482196—

Reaction Steps

To 1.1 g. of 1-(2-methylamino-5-nitrobenzoyl)-1H-indazol-3-ol, prepared in Example 14, suspended in 200 ml of absolute EtOH was added 200 mg of 5% Pd/C and the mixture was hydrogenated at 50 psi for 16 hours. The catalyst was filtered off, washed with hot EtOH and the filtrate was diluted with H2O and concentrated to small volume. The precipitate was collected, washed with cold 95% EtOH and dried; yield of dark-yellow amorphous powder 0.65 g. (65.4%); m.p. 184°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537966
Source datasetuspto-grants-1985_08
ORD IDord-2e1ea073a0d54675ae6a193630976836
Source noteuspto-grants-1985_08