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Methylamine → 2,5-dichloro-N-methylpyrimidin-4-amine

HRID 1503294
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HRID 1503294 반응식
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([Cl:9])=[CH:4][N:3]=1.[CH3:10][NH2:11]>CO>[Cl:1][C:2]1[N:7]=[C:6]([NH:11][CH3:10])[C:5]([Cl:9])=[CH:4][N:3]=1
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참가 물질

4

반응물 2

HCID 6329MethylamineHCID 2372592,4,5-Trichloropyrimidine

생성물 1

HCID 189812472,5-dichloro-N-methylpyrimidin-4-amine수율 50%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a cooled (0° C.) solution of 2,4,5-trichloropyrimidine (2.0 g, 11 mmol) in methanol (30 mL) was added dropwise a 2 M solution of methylamine in methanol (6.3 mL). The reaction was allowed to warm to room temperature and stirred overnight. The reaction was then concentrated and redissolved in DCM. The solution was washed with sat. NaHCO3, brine, dried over Na2SO4, filtered and concentrated. The crude product was purified by column chromatography (0-40% EtOAc in heptane) to give 2,5-dichloro-N-methylpyrimidin-4-amine (0.9 g, 50%). 1H-NMR (DMSO): δ 8.13 (s, 1H), 7.89 (s, 1H), 2.86 (d, J=4.5, 3H).

후처리

  1. concentrationThe reaction was then concentrated
  2. dissolutionredissolved in DCM
  3. washThe solution was washed with sat. NaHCO3, brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by column chromatography (0-40% EtOAc in heptane)

출처 및 근거

ORD 기록
ord-622ad1055fe1431982bee4d940f0ebd9
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09212173B2

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