Water → (3S,6R)-1-(2-Amino-6-chloro-4-pyrimidinyl)-6-methyl-N-phenyl-3-piperidinecarboxamide

HRID 2367416노트

반응식

HRID 2367416 반응식
[CH3:1][C@H:2]1[NH:7][CH2:6][C@@H:5]([C:8]([NH:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:9])[CH2:4][CH2:3]1.[Cl:17][C:18]1[CH:23]=[C:22](Cl)[N:21]=[C:20]([NH2:25])[N:19]=1.C([O-])(O)=O.[Na+].O>O1CCOCC1.CCOC(C)=O.ClC1C=C(Cl)N=C(N)N=1>[NH2:25][C:20]1[N:21]=[C:22]([N:7]2[C@H:2]([CH3:1])[CH2:3][CH2:4][C@H:5]([C:8]([NH:10][C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)=[O:9])[CH2:6]2)[CH:23]=[C:18]([Cl:17])[N:19]=1

참가 물질

8

실험 절차

To a solution of (3S,6R)-6-methyl-N-phenyl-3-piperidinecarboxamide (12 g, 55 mmol) in 1,4-dioxane (250 mL) was added 4,6-dichloro-2-pyrimidinamine (8.11 g, 49.5 mmol) and sat. aqueous NaHCO3 (125 mL), and the reaction mixture was then refluxed overnight. The reaction was not completed. The reaction mixture was cooled, added 4,6-dichloro-2-pyrimidinamine (0.9 g, 5.5 mmol), and refluxed overnight. When the reaction was completed, the mixture was cooled down. To the mixture was added about 500 mL of H2O to form a precipitate, and then filtered to obtain a gummy solid. The gummy solid was then dissolved in EtOAc (˜800 mL). The organic solution was washed with water (2×200 mL), brine (200 mL), dried (Na2SO4), filtered, and concentrated in vacuo to afford the crude title compound (20 g). LC-MS (ES) m/z=346 [M+H]+.

후처리

  1. temperaturethe reaction mixture was then refluxed overnight
  2. temperatureThe reaction mixture was cooled
  3. temperaturerefluxed overnight
  4. temperaturethe mixture was cooled down
  5. customto form a precipitate
  6. filtrationfiltered
  7. customto obtain a gummy solid
  8. washThe organic solution was washed with water (2×200 mL), brine (200 mL)
  9. dry with materialdried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7200e9f940fe45cf9c640dce67bd19cf
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08697685B2

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