Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362138Generated: October 30, 2026

HCID 86753712, compound → HCID 53909103, compound

https://huagongshe.com/reaction/362138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86753712HCID 86753712—
SolventWaterHCID 962—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 53909103HCID 5390910377.4%

Reaction Steps

49 mg (0.046 mmol) of N2-[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]-N1-[1(S)-(dimethoxymethyl)-3-pentynyl]-L-leucinamide were dissolved in 4 ml of trifluoroacetic acid/dichloromethane (1:1) containing3 drops of water and the solution was stirred for 1 hour under a nitrogen atmosphere. The solution was evaporated to dryness under a vacuum and the residue was re-evaporated twice with toluene. The solid was triturated with 10 ml of diethyl ether to give 30 mg of 2(S)-[[N-[N-[N-[N-[N-(3-carboxypropionyl)-L-α-aspartyl]-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucyl]amino]-4-hexynal as a white solid; MS: m/e 843.6 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-ab3ebad2114d42d0a9149afc7c50504b
Source noteuspto-grants-1999_02