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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516340생성일: 2026년 10월 23일

4-(4-chloro-6-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-1,3,5-triazin-2-yl)morpholine → HCID 67543796, 화합물

https://huagongshe.com/ko/reaction/516340

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-chloro-6-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-1,3,5-triazin-2-yl)morpholineHCID 22036872—
반응물tert-Butyl 4-(3-hydroxypropylamino)piperidine-1-carboxylateHCID 43652169—
용매DimethylformamideHCID 6228—
용매DiisopropylethylamineHCID 81531—
생성물HCID 67543796HCID 6754379683%

반응 단계

Reaction of 1-[4-chloro-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-1H-benzimidazole (WO 2006/095906) with tert-butyl 4-[(3-hydroxypropyl)amino]-1-piperidinecarboxylate in DMF and DIPEA as in Example 21 gave tert-butyl 4-[[4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(4-morpholinyl)-1,3,5-triazin-2-yl](3-hydroxypropyl)amino]-1-piperidinecarboxylate in 83% yield: mp (CH2Cl2/hexanes) 188-190° C.; 1H NMR (DMSO-d6) (rotamers) δ 8.45 and 8.35 (2d, J=7.9, 8.3 Hz, 1H), 7.83 and 7.75 (2t, JHF=52.9 Hz, 1H), 7.85 (2d, J=8.0 Hz, 1H), 7.54-7.41 (m, 2H), 4.72-4.65 and 4.56-4.51 (2m, 1H), 4.58 and 4.48 (2t, J=4.8, 5.0 Hz, 1H), 4.15-4.07 (m, 2H), 3.83-3.78 (m, 4H), 3.70 (m, 4H), 3.62-3.47 (m, 4H), 2.81 (m, 2H), 1.78-1.65 (m, 6H), 1.42 (s, 9H); Anal Calcd. for C28H38F2N8O4: C, 57.1; H, 6.5; N, 19.0. Found: C, 57.4; H, 6.3; N, 19.1%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108980B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-d1745284d5574675818a90dda07cb57a
출처 메모uspto-grants-2015_08