(R)-tert-butyl 3-((4-(5-(2,6-difluorophenyl)-1H-indol-3-yl)-6-methoxypyrimidin-2-yl)amino)piperidine-1-carboxylate → (R)-6-(5-(2,6-difluorophenyl)-1H-indol-3-yl)-2-(piperidin-3-ylamino)pyrimidin-4(3H)-one

HRID 1529426노트

반응식

HRID 1529426 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[C:12]2[C:18]1[CH:23]=[C:22]([O:24]C)[N:21]=[C:20]([NH:26][C@@H:27]2[CH2:32][CH2:31][CH2:30][N:29](C(OC(C)(C)C)=O)[CH2:28]2)[N:19]=1>Br.CC(O)=O>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[C:12]2[C:18]1[N:19]=[C:20]([NH:26][C@@H:27]2[CH2:32][CH2:31][CH2:30][NH:29][CH2:28]2)[NH:21][C:22](=[O:24])[CH:23]=1

참가 물질

4

실험 절차

A solution of (R)-tert-butyl 3-((4-(5-(2,6-difluorophenyl)-1H-indol-3-yl)-6-methoxypyrimidin-2-yl)amino)piperidine-1-carboxylate (0.17 g, 0.318 mmol) in 33% HBr in HOAc (3 mL) was heated at 90° C. for 14 h. The reaction was quenched with aq. NaHCO3 and extracted with EtOAc. The organic layer was dried (Na2SO4), filtered and concentrated. The residue was washed with 50% EtOAc in petroleum ether to give (R)-6-(5-(2,6-difluorophenyl)-1H-indol-3-yl)-2-(piperidin-3-ylamino)pyrimidin-4(3H)-one (30 mg, 22%). MS (ESI, pos. ion) m/z: 422.1 (M+1); 1H-NMR (400 MHz DMSO-d6): δ ppm 11.78 (s, 1H), 8.48 (s, 1H), 8.13 (d, J=2.4 Hz, 1H), 7.53 (d, J=8.8 Hz, 1H), 7.40-7.47 (m, 1H), 7.18-7.22 (m, 3H), 6.59 (brs, 1H), 6.00 (s, 1H), 3.93 (brs, 1H), 2.57 (s, 2H), 2.90 (d, J=9.2 Hz, 1H), 1.74 (brs, 1H), 1.50-1.53 (m, 2H), 1.18-1.22 (m, 3H).

후처리

  1. customThe reaction was quenched with aq. NaHCO3
  2. extractionextracted with EtOAc
  3. dry with materialThe organic layer was dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. washThe residue was washed with 50% EtOAc in petroleum ether

출처 및 근거

ORD 기록
ord-3cca105d3a624277bea0f26831daf580
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09090593B2

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