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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362149Generated: October 29, 2026

HCID 22942118, compound → HCID 22942119, compound

https://huagongshe.com/reaction/362149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22942118HCID 22942118—
CatalystPalladiumHCID 23938—
ProductHCID 22942119HCID 2294211997.8%

Reaction Steps

A solution of 230 mg (0.223 mmol) of N-[N-[N-[N-[N-[3-(tert-butoxycarbonyl)propionyl]-O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-3-cyclopentyl-L-alanine benzyl ester in 10 ml of dimethylformamidewas hydrogenated over 25 mg of 10% palladium/carbon for 3 hours. The catalyst was removed by filtration, the filtrate was evaporated and the residue was triturated with diethyl ether to give 206 mg of N-[N-[N-[N-[N-[3-(tert-butoxycarbonyl)propionyl]-O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-3-cyclopentyl-L-alanine as a white solid; MS: m/e 944 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-2caf32eaad694a7aae59ccb1e4120172
Source noteuspto-grants-1999_02