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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189387Generated: October 30, 2026

4-[(4-{3-[(S)-5-Benzyloxycarbonylamino-1-(carbamoyl)pentylamino]propoxy}-2-methylphenyl)methyl]-3-(beta-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazole → 4-[(4-(3-[(S)-5-Amino-1-(carbamoyl)pentylamino]propoxy)-2-methylphenyl)methyl]-3-(beta-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazole

https://huagongshe.com/reaction/2189387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(4-{3-[(S)-5-Benzyloxycarbonylamino-1-(carbamoyl)pentylamino]propoxy}-2-methylphenyl)methyl]-3-(beta-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazoleHCID 68941036—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product4-[(4-(3-[(S)-5-Amino-1-(carbamoyl)pentylamino]propoxy)-2-methylphenyl)methyl]-3-(beta-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazoleHCID 1041605593.7%

Reaction Steps

To a solution of 4-[(4-{3-[(S)-5-benzyloxycarbonylamino-1-(carbamoyl)pentylamino]propoxy}-2-methylphenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazole (0.17 g) in methanol (4 mL) was added 10% palladium-carbon powder (30 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere for 1 hour. The insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure to give the title compound (0.13 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324176B2
Source datasetuspto-grants-2012_12
ORD IDord-3c0666c6b87d412d86d26a8c1d8a7ddc
Source noteuspto-grants-2012_12