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Phosphorus oxychloride → 7-Chloro-2-(4-fluorophenyl)-oxazolo[5,4-d]pyrimidine

HRID 1396735
ノート
印刷プレビュー

反応式

HRID 1396735 の反応式
O[C:2]1[C:7]([NH:8][C:9](=[O:17])[C:10]2[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=2)=[C:6](O)[N:5]=[CH:4][N:3]=1.C(N(C(C)C)CC)(C)C.O=P(Cl)(Cl)[Cl:30]>>[Cl:30][C:6]1[C:7]2[N:8]=[C:9]([C:10]3[CH:11]=[CH:12][C:13]([F:16])=[CH:14][CH:15]=3)[O:17][C:2]=2[N:3]=[CH:4][N:5]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 24813Phosphorus oxychlorideHCID 81531DiisopropylethylamineHCID 178522470HCID 178522470、化合物

生成物 1

HCID 866624407-Chloro-2-(4-fluorophenyl)-oxazolo[5,4-d]pyrimidine収率 30%

反応条件

温度
90 °C

実験手順

To a solution of N-(4,6-dihydroxypyrimidin-5-yl)-4-fluorobenzamide (0.30 g, 1.20 mmol) in POCl3 (6 ml) was added diisopropylethylamine (0.42 ml, 2.41 mmol). The reaction mixture was stirred under N2 at 90° C. for 3.5 hours. The reaction mixture was allowed to cool down to room temperature and the volatiles were evaporated to dryness. The residue was diluted with water and the aqueous phase was extracted with diethyl ether. The combined organic layers were washed with a saturated NaHCO3 solution and brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel (CH2Cl2/MeOH 100:1) to yield the title compound as a white solid (0.13 g, 30%).

後処理

  1. temperatureto cool down to room temperature
  2. customthe volatiles were evaporated to dryness
  3. additionThe residue was diluted with water
  4. extractionthe aqueous phase was extracted with diethyl ether
  5. washThe combined organic layers were washed with a saturated NaHCO3 solution and brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by chromatography on silica gel (CH2Cl2/MeOH 100:1)

出典と根拠

ORDレコード
ord-201d20b98e814882829147fbbd3214da
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08901132B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート