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Phosphorus oxychloride → 4-Chloro-6-phenylfuro[2,3-d]pyrimidine

HRID 2408976
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HRID 2408976 반응식
[C:1]1([C:7]2[O:16][C:10]3[N:11]=[CH:12][NH:13][C:14](=O)[C:9]=3[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O=P(Cl)(Cl)[Cl:19]>>[Cl:19][C:14]1[C:9]2[CH:8]=[C:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[O:16][C:10]=2[N:11]=[CH:12][N:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 580167996-phenylfuro[2,3-d]pyrimidin-4(3H)-one

생성물 1

HCID 579464884-Chloro-6-phenylfuro[2,3-d]pyrimidine수율 74%

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온도
60 °C

실험 절차

A mixture of 6-phenylfuro[2,3-d]pyrimidin-4(3H)-one (1.0 g) and POCl3 (10 mL) was stirred at 55-65° C. for 3 h. The reaction mixture was poured into ice cold water and stirred for 10 min. The solution was extracted with chloroform (3×100 mL) and the combined chloroform layer was washed with aq. NaHCO3 solution, water, brine and dried over sodium sulfate. The residue was chromatographed over silica gel column using hexane-EtOAc (95:5) as eluents to give the product as a white color solid (800 mg, 74%), mp 136-138° C. 1H NMR (400 MHz, CDCl3): δ 8.74 (1H, s), 7.90-7.93 (2H, m), 7.45-7.54 (3H, m), 7.08 (1H, s).

후처리

  1. additionThe reaction mixture was poured into ice cold water
  2. stirringstirred for 10 min
  3. extractionThe solution was extracted with chloroform (3×100 mL)
  4. washthe combined chloroform layer was washed with aq. NaHCO3 solution, water, brine
  5. dry with materialdried over sodium sulfate
  6. customThe residue was chromatographed over silica gel column

출처 및 근거

ORD 기록
ord-10807ee8d23149ff95cb5f2720371fa2
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815879B2

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