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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386569Generated: October 31, 2026

HCID 86757194, compound → HCID 86757193, compound

https://huagongshe.com/reaction/1386569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86757194HCID 86757194—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86757193HCID 8675719369%

Reaction Steps

A solution of 0.15 g of (E)-2′-(3-aminopropanesulphonyl)-2(R)-[1(S)-(benzyloxycarbamoyl)-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in 5 ml of methanol was hydrogenated in the presence of 60 mg of 10% palladium-on-charcoal until uptake of hydrogen was complete. The catalyst was removed by filtration and the solvent was evaporated. The residue was triturated with diethyl ether and there was obtained 0.088 g of 2′-(3-aminopropanesulphonyl)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenylbutyl]-2′-isobutyl-4-methylvalerohydrazide in the form of a pale pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265446B1
Source datasetuspto-grants-2001_07
ORD IDord-37cdaea86e6d4acc81871010f3f4f4f9
Source noteuspto-grants-2001_07