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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1272970생성일: 2026년 10월 27일

N-(3-{1-Perhydro-2H-pyran-2-yl-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)](1H-indazol-3-yl)}phenyl)-3-phenylpropanamide → N-[3-(5-(1H-1,2,4-Triazol-3-Yl)(1H-Indazol-3-Yl))Phenyl]-3-Propanamide

https://huagongshe.com/reaction/1272970

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-{1-Perhydro-2H-pyran-2-yl-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)](1H-indazol-3-yl)}phenyl)-3-phenylpropanamideHCID 22480348—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
생성물N-[3-(5-(1H-1,2,4-Triazol-3-Yl)(1H-Indazol-3-Yl))Phenyl]-3-PropanamideHCID 17846002348%

반응 단계

N-(3-{1-perhydro-2H-pyran-2-yl-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)](1H-indazol-3-yl)}phenyl)-3-phenylpropanamide was dissolved in 4 mL of 4.0 N HCl in 1,4-dioxane and the reaction was stirred at room temperature overnight. After neutralization with aqueous NaHCO3, the crude product was extracted in ethyl acetate and purified by preparative HPLC (0.049 g, 48% yield over 2 steps): 1H NMR (CD3OD) δ 8.73 (s, 1H), 8.40 (br s, 2H), 8.16 (s, 1H), 8.10 (d, 1H), 7.77–7.67 (m, 3H), 7.50 (t, 1H), 7.28 (d, 4H), 7.18 (sextet, 1H); ES-MS (m/z) 409.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07208513B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-edb312ffd56f42119e726d2086dae8ed
출처 메모uspto-grants-2007_04