HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Benzofurancarbonyl chloride → HCID 68710769, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Benzofurancarbonyl chloride | HCID 38949 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | methyl N-[(4'-amino-1,1'-biphenyl-4-yl)sulfonyl]-N-methyl-D-valinate | HCID 59150916 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 68710769 | HCID 68710769 | 86,6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07420001B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-0587f10292e2495193029e1e95053a0f |
| Quellennotiz | uspto-grants-2008_09 |