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Methylamine → 2-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine

HRID 1503472
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HRID 1503472 반응식
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1.[CH2:13]([N:15](CC)CC)C.CN>CO>[Cl:1][C:2]1[N:7]=[C:6]([NH:15][CH3:13])[C:5]([C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1
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참가 물질

5

반응물 3

HCID 6329MethylamineHCID 8471TriethylamineHCID 27827742,4-Dichloro-5-(trifluoromethyl)pyrimidine

생성물 1

HCID 210775872-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine수율 45.7%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a cooled (−10° C.) solution of 2,4-dichloro-5-trifluoromethylpyrimidine (20 g, 0.089 mol) in methanol (100 mL) was added triethylamine (12.5 mL, 0.089 mol) and a 2 M solution of methylamine in methanol (45 mL). The reaction was allowed to warm to room temperature and stirred overnight. The reaction was then concentrated and re-dissolved in ethyl acetate. The solution was washed with sat. NaHCO3, brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (5-25% EtOAc in heptane) to give 2-chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine (8.6 g, 45%). 1H-NMR (DMSO): δ 8.37 (s, 1H), 7.90 (s, 1H), 2.90 (s, 3H).

후처리

  1. concentrationThe reaction was then concentrated
  2. dissolutionre-dissolved in ethyl acetate
  3. washThe solution was washed with sat. NaHCO3, brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by column chromatography (5-25% EtOAc in heptane)

출처 및 근거

ORD 기록
ord-5319360eef6741a2b551cfc8dd76b9e2
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09212186B2

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