Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl (2R)-4-{4'-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoate → (2R)-4-{4'-[(Di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl (2R)-4-{4'-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoate | HCID 66577870 | — |
| 반응물 | HCID 86668761 | HCID 86668761 | — |
| 생성물 | (2R)-4-{4'-[(Di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoic acid | HCID 66577853 | 81% |
반응 단계
The title compound (4.44 g, 81%) was prepared from ethyl(2R)-4-{4′-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoate (5.8 g, 10.2 mmol) by following a procedure analogous to that described for the preparation of 4-(6-bromopyridin-3-yl)-2-methyl-2-(methylsulfonyl)butanoic acid (i.e. Example 3, Step D). MS (LCMS) m/z 539.5 (M−1). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.53-1.57 (m, 18H) 1.69 (s, 3H) 2.09-2.18 (m, 1H) 2.38-2.53 (m, 2H) 2.62-2.73 (m, 1H) 3.05 (s, 3H) 7.10 (d, J=8.20 Hz, 2H) 7.25-7.37 (m, 4H) 7.45-7.51 (m, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08853258B2 |
| 출처 데이터셋 | uspto-grants-2014_10 |
| ORD ID | ord-f03c9f41c73c45ed9952b4a66168786b |
| 출처 메모 | uspto-grants-2014_10 |