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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223979Generated: October 29, 2026

HCID 86614401, compound → HCID 86614400, compound

https://huagongshe.com/reaction/2223979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86614401HCID 86614401—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 86614400HCID 8661440099.8%

Reaction Steps

To a solution of 4-[2-(4-{(E)-3-[l-{[4-(benzyloxy-carbonyl)piperazin-1-yl]carbonyl}-1-(methyl)ethyl-carbamoyl]prop-1-enyl}phenyl)ethynyl]-3-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-indazole (34 mg) in methanol (3 mL) was added 10% palladium-carbon powder (10 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere for 2 hours. The insoluble material was removed by filtration, and the solvent of the filtrate was removed under reduced pressure to give 4-{2-[4-(3-{1-[(piperazin-1-yl)-carbonyl]-1-(methyl)ethylcarbamoyl}propyl)phenyl]ethyl}-3-(2,3,4, 6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-indazole (30 mg). This material was dissolved in methanol (3 mL). To the solution was added lithium hydroxide monohydrate (6 mg), and the mixture was stirred at room temperature overnight. To the reaction mixture was added acetic acid (0.1 mL), and the resulting mixture was concentrated under reduced pressure. The residue was purified by solid phase extraction on ODS (washing solvent: distilled water, eluent:methanol) to give the title compound (17 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375113B2
Source datasetuspto-grants-2008_05
ORD IDord-f98ae1f40b3842439cd2ef8854a13cb2
Source noteuspto-grants-2008_05