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Phosphorus oxychloride → 3-Benzyl-5-chloro-8-methylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione

HRID 2067734
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HRID 2067734 반응식
[CH2:1]([N:8]1[C:13](=[O:14])[C:12]2[C:15](O)=[CH:16][C:17](=[O:20])[N:18]([CH3:19])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:24]>>[CH2:1]([N:8]1[C:13](=[O:14])[C:12]2[C:15]([Cl:24])=[CH:16][C:17](=[O:20])[N:18]([CH3:19])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 598230373-Benzyl-5-hydroxy-8-methylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione

생성물 1

HCID 598230573-Benzyl-5-chloro-8-methylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione수율 94%

실험 절차

3-Benzyl-5-hydroxy-8-methylpyrido[2,3-d]pyrimidine-4,7(3H,8H)-dione (1.1 g, 3.88 mmol) was dissolved in excess POCl3 (5 mL) and subjected to microwave irradiation at 70° C. for 30 minutes. The POCl3 was removed in vacuo and the residue dissolved in DCM then quickly washed with saturated sodium bicarbonate solution until neutral pH was observed. The organic layer was dried over MgSO4 and evaporated to dryness to give 1.5 g of the title compound as a reddish brown solid (94%). [M+H] calc'd for C15H12ClN3O, 302; found, 302.

후처리

  1. custom
irradiation at 70° C. for 30 minutes
  • customThe POCl3 was removed in vacuo
  • dissolutionthe residue dissolved in DCM
  • washthen quickly washed with saturated sodium bicarbonate solution until neutral pH
  • dry with materialThe organic layer was dried over MgSO4
  • customevaporated to dryness
  • 출처 및 근거

    ORD 기록
    ord-182dab78acb647079b187f036c786374
    출처 데이터셋
    uspto-grants-2012_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08293901B2

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