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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850883Generated: October 31, 2026

HCID 86753712, compound → HCID 53909103, compound

https://huagongshe.com/reaction/850883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86753712HCID 86753712—
CatalystWaterHCID 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) containing 3 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 numberUS06018020
Source datasetuspto-grants-2000_01
ORD IDord-7064103c369a41ed8beea4e779337d1a
Source noteuspto-grants-2000_01