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Diisopropylethylamine → 4-Chloro-N-methyl-6-[(3R)-3-methyl-4-morpholinyl]-2-pyrimidinamine

HRID 2367533
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HRID 2367533 반응식
Cl[C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([NH:9][CH3:10])[N:3]=1.CCN(C(C)C)C(C)C.[CH3:20][C@@H:21]1[CH2:26][O:25][CH2:24][CH2:23][NH:22]1>C(O)C>[Cl:8][C:6]1[CH:7]=[C:2]([N:22]2[CH2:23][CH2:24][O:25][CH2:26][C@H:21]2[CH3:20])[N:3]=[C:4]([NH:9][CH3:10])[N:5]=1
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 2598804,6-Dichloro-n-methylpyrimidin-2-amineHCID 641498(R)-3-Methylmorpholine

생성물 1

HCID 585047304-Chloro-N-methyl-6-[(3R)-3-methyl-4-morpholinyl]-2-pyrimidinamine수율 68.7%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
100 °C

실험 절차

To a solution of 4,6-dichloro-N-methyl-2-pyrimidinamine (2 g, 11.23 mmol) in ethanol (50 mL) in a 200-mL RBF were added Hunig's base (5.89 mL, 33.7 mmol) and (3R)-3-methylmorpholine (1.546 g, 11.23 mmol). The reaction mixture was stirred at 100° C. in a sealed tube on a stirrer hotplate for 2 days. The reaction was concentrated in vacuo, and the residue was dissolved in EtOAc (200 mL) and washed with water (50 mL). The organic layer was dried over Na2SO4, filtered, then concentrated to afford the title compound (1.873 g) as a white solid. LC-MS (ES) m/z=243 [M+H]+.

후처리

  1. concentrationThe reaction was concentrated in vacuo
  2. dissolutionthe residue was dissolved in EtOAc (200 mL)
  3. washwashed with water (50 mL)
  4. dry with materialThe organic layer was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-79f51be833284e2fa2f112c514254ce2
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08697685B2

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