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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362155Generated: October 30, 2026

Dichloromethane → HCID 22942064, compound

https://huagongshe.com/reaction/362155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHCID 22942110HCID 22942110—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 22942064HCID 22942064121.8%

Reaction Steps

200 mg (0.18 mmol) of N2-[N-[N-[N-[N-(tert-butoxycarbonyl)-O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-N1-[4-fluoro-1(RS)-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butyl]-L-leucinamide were dissolved in 4.75 ml of trifluoroacetic acid and 0.25 ml of water. 2 ml of dichloromethane were added and the solution was stirred at room temperature for 3 hours. The solution was diluted with toluene and evaporated. The residue was triturated with diethyl ether and the resulting solid was filtered off and dried to give 95 mg of 4-fluoro-1(RS)-[[N-[N-[N-[N-[N-(3-carboxypropionyl)-L-α-aspartyl]-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucyl]amino]butylboronic acid; MS: m/e 849.4 [M+H-H2O]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-056747104bdb4522a500b788d2d80f07
Source noteuspto-grants-1999_02