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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29316Erstellt: 24. Oktober 2026

2-Benzofurancarbonyl chloride → HCID 68710769, Verbindung

https://huagongshe.com/de/reaction/29316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Benzofurancarbonyl chlorideHCID 38949—
EduktDiisopropylethylamineHCID 81531—
Eduktmethyl N-[(4'-amino-1,1'-biphenyl-4-yl)sulfonyl]-N-methyl-D-valinateHCID 59150916—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 68710769HCID 6871076986,6%

Reaktionsschritte

To 0.11 g of methyl N-[(4′-amino-1,1′-biphenyl-4-yl)sulfonyl]-N-methyl-D-valinate in 4 mL dichloromethane cooled in ice bath, was added 0.058 g of 2-benzofurancarbonyl chloride, and N,N-diisopropylethylamine (0.15 mL) was dropped in. The reaction was stirred at room temperature overnightand then diluted with dichloromethane. The organic layer was washed with water, 5% HCl, and brine, dried over sodium sulfate, filtered, concentrated, and purified by column chromatography eluting with hexane:ethyl acetate (2:1) to provide 0.13 g of methyl N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)-N-methyl-D-valinate. Yield 86.6%. m.p. 67-69° C. MS: 521.3 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420001B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-0587f10292e2495193029e1e95053a0f
Quellennotizuspto-grants-2008_09