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Phosphorus oxychloride → 2-Methyl-5-propyl-6-chloro-pyrimidine-4-carboxylic acid ethyl ester

HRID 916643
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HRID 916643 반응식
[CH2:1]([O:3][C:4]([C:6]1[C:11]([CH2:12][CH2:13][CH3:14])=[C:10](O)[N:9]=[C:8]([CH3:16])[N:7]=1)=[O:5])[CH3:2].O=P(Cl)(Cl)[Cl:19]>>[CH2:1]([O:3][C:4]([C:6]1[C:11]([CH2:12][CH2:13][CH3:14])=[C:10]([Cl:19])[N:9]=[C:8]([CH3:16])[N:7]=1)=[O:5])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178439777HCID 178439777, 화합물

생성물 1

HCID 233941042-Methyl-5-propyl-6-chloro-pyrimidine-4-carboxylic acid ethyl ester

반응 조건

온도
85 °C

실험 절차

A mixture of 121 (10 mmol) and POCl3 (25 ml) is heated at 85° C. for 4 hours. The solvent is removed in vacuo and EtOAc (40 ml) and water (30 ml) are added to the residue. NaHCO3 is carefully added until the pH of the aqueous layer is greater than 7. The layers are separated and the aqueous layer is extracted with EtOAc (2×30 ml). The combined extracts are washed with brine (50 ml), dried (Na2SO4) and evaporated. Flash column purification of the residue with 3:1 EtOAc, hexane provides the product (122) as a light yellow oil.

후처리

  1. custom
The solvent is removed in vacuo and EtOAc (40 ml) and water (30 ml)
  • additionare added to the residue
  • additionNaHCO3 is carefully added until the pH of the aqueous layer
  • customThe layers are separated
  • extractionthe aqueous layer is extracted with EtOAc (2×30 ml)
  • washThe combined extracts are washed with brine (50 ml)
  • dry with materialdried (Na2SO4)
  • customevaporated
  • customFlash column purification of the residue with 3:1 EtOAc, hexane
  • 출처 및 근거

    ORD 기록
    ord-373f08c2b5304eb88c7ce7cb3c5524b3
    출처 데이터셋
    uspto-grants-2007_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07271170B2

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