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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2091835생성일: 2026년 10월 27일

2-cyclopropyl-1H-1,3-benzodiazole → 2-(1-((2-(2-cyclopropyl-1H-benzo[d]imidazol-1-yl)-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-ol

https://huagongshe.com/reaction/2091835

반응식

참여 물질

역할이름HCID투입량
반응물2-cyclopropyl-1H-1,3-benzodiazoleHCID 1084419—
반응물2-(1-((2-Chloro-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-olHCID 58404970—
생성물2-(1-((2-(2-cyclopropyl-1H-benzo[d]imidazol-1-yl)-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-olHCID 53377949—

반응 단계

Following General Procedure C, 2-cyclopropyl-benzimidazole and 2-(1-((2-chloro-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-ol from Example 8 were reacted to give 102. LCMS (MH+)=528.3. 1H-NMR (DMSO-d6): δ 8.19 (d, 1H), 8.03 (m, 1H), 7.89 (d, 1H), 7.44 (m, 1H), 7.23 (m, 2H), 4.56 (s, 4H), 4.01 (s, 1H), 3.83 (m, 4H), 3.74 (2, 2H), 2.94 (m, 3H), 1.99 (m, 2H), 1.67 (m, 2H), 1.29 (m, 2H), 1.16 (m, 3H), 1.08 (m, 2H), 1.04 (s, 6H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08440651B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-95d104a268c24e94b7d0202ab8ca6d8c
출처 메모uspto-grants-2013_05