Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl]methanesulfonamide → N-{6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl]methanesulfonamide | HCID 17978472 | — |
| 반응물 | 6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-ylamine | HCID 17978566 | — |
| 용매 | Ethylacetate heptane | HCID 21899848 | — |
| 생성물 | N-{6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide | HCID 17978608 | — |
반응 단계
N-{6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide was prepared as described for N-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl] methane sulfonamide in Example 46 starting from 442 mg of 6-[2-(4-fluorophenyl)-chroman-6-yloxy]-pyridin-3-ylamine (Example 76). The product was passed through silica gel using ethyl acetate-heptane (10:3) as an eluant and then crystallised from diethyl ether. 1H NMR (400 MHz, CDCl3) δ: 8.09 (d, 1H, J 2.8 Hz), 7.72 (dd, 1H, J 8.9, 2.8 Hz), 7.40 (m, 2H), 7.08 (m, 2H), 6.92-6.87 (m, 4H), 6.74 (s, 1H), 5.03 (dd, 1H, J 10.4, 2.3 Hz), 3.01 (m, 1H), 3.00 (s, 3H), 2.80 (m, 1H), 2.19 (m, 1H), 2.07 (m, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07425568B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-5ff2e3f6a2534af2b608d0b3dcc8ae6f |
| 출처 메모 | uspto-grants-2008_09 |