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

HRID 965685
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HRID 965685 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]
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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

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온도
85 °C

실험 절차

A mixture of 2-methyl-5-propyl-6-hydroxy-pyrimidine-4-carboxylic acid ethyl ester (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 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 2-methyl-5-propyl-6-chloro-pyrimidine-4-carboxylic acid ethyl ester as a light yellow oil. Step 4. Preparation of 2-Methyl-5-propyl-4-chloromethyl-6-chloro-pyrimidine

후처리

  1. customThe solvent is removed in vacuo and EtOAc (40 mL) and water (30 mL)
  2. additionare added to the residue
  3. additionNaHCO3 is carefully added until the pH of aqueous layer
  4. customThe layers are separated
  5. extractionthe aqueous layer is extracted with EtOAc (2×30 mL)
  6. washThe combined extracts are washed with brine (50 mL)
  7. dry with materialdried (Na2SO4)
  8. customevaporated
  9. customFlash column purification of the residue with 3:1 EtOAc, hexane

출처 및 근거

ORD 기록
ord-517ddb9926014f848dd7403fe75c1b53
출처 데이터셋
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06951864B2

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