Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Benzofurancarbonyl chloride → HCID 68710769, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Benzofurancarbonyl chloride | HCID 38949 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | methyl N-[(4'-amino-1,1'-biphenyl-4-yl)sulfonyl]-N-methyl-D-valinate | HCID 59150916 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | HCID 68710769 | HCID 68710769 | 86.6% |
반응 단계
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)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07420001B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-0587f10292e2495193029e1e95053a0f |
| 출처 메모 | uspto-grants-2008_09 |