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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171322생성일: 2026년 10월 26일

1-Aminocyclopentanemethanol → 3-Fluoro-N-{4-[(2-{[1-(hydroxymethyl)cyclopentyl]amino}pyrimidin-4-yl)oxy]-1-naphthyl}-5-piperidin-1-ylbenzamide

https://huagongshe.com/reaction/1171322

반응식

참여 물질

역할이름HCID투입량
반응물1-AminocyclopentanemethanolHCID 66307—
반응물3-fluoro-N-[4-(2-methanesulfonyl-pyrimidin-4-yloxy)-naphthalen-1-yl]-5-piperidin-1-yl-benzamideHCID 66737969—
생성물3-Fluoro-N-{4-[(2-{[1-(hydroxymethyl)cyclopentyl]amino}pyrimidin-4-yl)oxy]-1-naphthyl}-5-piperidin-1-ylbenzamideHCID 59553331—

반응 단계

Compound is prepared from 3-fluoro-N-[4-(2-methanesulfonyl-pyrimidin-4-yloxy)-naphthalen-1-yl]-5-piperidin-1-yl-benzamide and 1-amino-cyclopentylmethanol according to conditions described in general procedure C. 1H NMR (400 MHz, DMSO-d6) δ 1.14 (s, 4 H), 1.58-1.61 (m, 10 H), 3.26-3.31 (m, 6 H), 6.27 (d, J=5.5 Hz, 1 H), 6.53 (s, 1 H), 6.95 (d, J=12.4 Hz, 1 H), 7.15 (d, J=8.8 Hz, 1 H), 7.35 (d, J=7.7 Hz, 1 H), 7.44 (s, 1 H), 7.52-7.59 (m, 3 H), 7.78 (s, 1 H), 7.95-7.97 (m, 1 H), 8.16 (d, J=5.5 Hz, 1 H), 10.41 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829560B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-43129639896448a9b02e993d1f8c5324
출처 메모uspto-grants-2010_11