Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Ethoxybenzoyl Chloride → 4-ethoxyphenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-gluco-pyranosyl)indol-3-yl ketone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Ethoxybenzoyl Chloride | HCID 140059 | — |
| 반응물 | 4-Fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indole | HCID 67020413 | — |
| 생성물 | 4-ethoxyphenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-gluco-pyranosyl)indol-3-yl ketone | HCID 67196421 | — |
반응 단계
4-Fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-indole obtained in Example 2-(3) and 4-ethoxybenzoyl chloride were treated in a manner similar to Example 2-(4) to give 4-ethoxyphenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-gluco-pyranosyl)indol-3-yl ketone as a colorless powder. APCI-Mass m/Z 614 (M+H). 1H-NMR (DMSO-d6) δ 1.38 (t, J=6.9 Hz, 3H), 1.68 (s, 3H), 1.97 (s, 3H), 1.98 (s, 3H), 2.04 (s, 3H), 4.11 (d, J=4.0 Hz, 2H), 4.16 (q, J=7.0 Hz, 2H), 4.28-4.31 (m, 1H), 5.30 (t, J=9.8 Hz, 1H), 5.54 (t, J=9.6 Hz, 1H), 5.76 (t, J=9.3 Hz, 1H), 6.34 (d, J=9.0 Hz, 1H), 7.01 (dd, J=10.6, 8.0 Hz, 1H), 7.07 (d, J=8.7 Hz, 2H), 7.36 (td, J=8.1, 4.9 Hz, 1H), 7.62 (d, J=8.3 Hz, 1H), 7.83 (d, J=8.8 Hz, 2H), 8.14 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07935674B2 |
| 출처 데이터셋 | uspto-grants-2011_05 |
| ORD ID | ord-96088ff4485742918b7d0be1aae3157d |
| 출처 메모 | uspto-grants-2011_05 |