Ethyl formate → 5-(2,4-Difluorophenoxy)-2-methylsulfanylpyrimidin-4-ol

HRID 575629

反応式

HRID 575629 の反応式
C([O:3][C:4](=O)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][C:8]=1[F:14])C.C(OCC)=O.[H-].[Na+].[O-]CC.[Na+].S(O)(O)(=O)=O.[CH3:32][S:33][C:34](=[NH:36])[NH2:35].[CH3:37]SC(=N)N>C1COCC1.CCO>[F:14][C:8]1[CH:9]=[C:10]([F:13])[CH:11]=[CH:12][C:7]=1[O:6][C:5]1[C:4]([OH:3])=[N:36][C:34]([S:33][CH3:32])=[N:35][CH:37]=1

参加物

8

実験手順

To a solution of 2-(2,4-difluorophenoxy)acetic acid ethyl ester (8.0 g, 37.01 mmol) and ethyl formate (4.11 g, 55.51 mmol) in dry THF (200 mL) was added NaH (1.55 g, 38.75 mmol) slowly at 0° C. The mixture was then refluxed for 2 h. In a separate flask, sodium ethoxide (3.02 g, 44.41 mmol) and S-methylthiopseudourea hemisulfate (6.17 g, 44.41 mmol) in EtOH (100 mL) were stirred at 20° C. for 2 h and then the resulting mixture was added to the above THF solution. The combined mixture was refluxed for 12 h. After concentration under vacuum, water (20 mL) and HCl (10 mL, aq. 1N) were added. The suspended solids were collected and washed with water (50 mL×3) and EtOH (50 mL×3) and dried to give the title compound (6.0 g, 60.0% yield) as a light yellow solid. 1H NMR (DMSO-d6, 400 MHz) δ 7.84 (s, 1H), 7.42-7.34 (m, 1H), 7.04-7.01 (m, 1H), 6.95 (t, J=9.6 Hz, 1H), 2.47 (s, 3H).

後処理

  1. temperatureThe mixture was then refluxed for 2 h
  2. temperatureThe combined mixture was refluxed for 12 h
  3. concentrationAfter concentration under vacuum, water (20 mL) and HCl (10 mL, aq. 1N)
  4. additionwere added
  5. customThe suspended solids were collected
  6. washwashed with water (50 mL×3) and EtOH (50 mL×3)
  7. customdried

出典と根拠

ORDレコード
ord-f375929d834d435b8136ef01d495846f
出典データセット
uspto-grants-2015_05
特許番号
US09034900B2

関連ノート

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