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Phosphorus oxychloride → 4-chloro-N-(1-methyl-1H-pyrazol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-amine

HRID 577701
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HRID 577701 반응식
[CH3:1][N:2]1[CH:6]=[C:5]([NH:7][C:8]2[N:9]=[C:10](O)[C:11]3[CH:16]=[CH:15][NH:14][C:12]=3[N:13]=2)[CH:4]=[N:3]1.O=P(Cl)(Cl)[Cl:20]>>[Cl:20][C:10]1[C:11]2[CH:16]=[CH:15][NH:14][C:12]=2[N:13]=[C:8]([NH:7][C:5]2[CH:4]=[N:3][N:2]([CH3:1])[CH:6]=2)[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178480794HCID 178480794, 화합물

생성물 1

HCID 866796464-chloro-N-(1-methyl-1H-pyrazol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-amine수율 56%

실험 절차

A solution of 2-((1-methyl-1H-pyrazol-4-yl)amino)-7H-pyrrolo[2,3-d]pyrimidin-4-ol (5 g, 0.02 mol) in POCl3 (50 mL) was stirred at 120° C. for 4 hrs. After removal of POCl3 by rotary evaporation, water (37 mL) was added. The pH was adjusted to 10 by aq. NaOH (2 mol/L, 30 mL) and then extracted with EtOAc/THF (2:1, three×200 mL). The combined organic layers were concentrated to dryness to afford the title compound (2.8 g, 56% yield) as a brown solid, which was used as is in the next step.

후처리

  1. customAfter removal of POCl3
  2. customby rotary evaporation, water (37 mL)
  3. additionwas added
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
extraction
extracted with EtOAc/THF (2:1, three×200 mL)
  • concentrationThe combined organic layers were concentrated to dryness
  • 출처 및 근거

    ORD 기록
    ord-4294898f8a49420ba0c5897e0975ba71
    출처 데이터셋
    uspto-grants-2015_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09040547B2

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