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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31295생성일: 2026년 10월 24일

N-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl]methanesulfonamide → N-{6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide

https://huagongshe.com/ko/reaction/31295

반응식

참여 물질

역할이름HCID투입량
반응물N-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl]methanesulfonamideHCID 17978472—
반응물6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-ylamineHCID 17978566—
용매Ethylacetate heptaneHCID 21899848—
생성물N-{6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425568B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5ff2e3f6a2534af2b608d0b3dcc8ae6f
출처 메모uspto-grants-2008_09