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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979230Generated: October 31, 2026

HCID 86756932, compound → HCID 86756931, compound

https://huagongshe.com/reaction/1979230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86756932HCID 86756932—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86756931HCID 8675693170.6%

Reaction Steps

A solution of 0.216 g of (E)-2(R)-[1(S)-(benzyloxycarbamoyl)-4-phenyl-3-butenyl]-2′-(4-benzyloxycarbonylaminobutyryl)-4-methyl-2′-(2(S)-methylbutyl)valerohydrazide in 5 ml of methanol was hydrogenated in the presence of 0.1 g of 10% palladium-on-carbon catalyst for 1 hour. The catalyst was removed by filtration and the methanol was evaporated. The residue was re-evaporated from diethyl ether and then triturated with a mixture of diethyl ether and hexane and there was obtained 0.104 g of 2′-(4-aminobutyryl)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenylbutyl]-4-methyl-2′-(2(S)-methylbutyl)valerohydrazide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239151B1
Source datasetuspto-grants-2001_05
ORD IDord-26bdf82b1f8741d497eb9226928fa08c
Source noteuspto-grants-2001_05