Water → 3-(3-{3-t-Butyl5-[3-(4-fluoro-phenyl)-ureido]-pyrazol-1-yl}-phenyl)-propionic acid ethyl ester

HRID 16956

反応式

HRID 16956 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][CH:3]=1.C1N=CN([C:14](N2C=NC=C2)=[O:15])C=1.[CH2:21]([O:23][C:24](=[O:43])[CH2:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[C:29]([N:33]2[C:37]([NH2:38])=[CH:36][C:35]([C:39]([CH3:42])([CH3:41])[CH3:40])=[N:34]2)[CH:28]=1)[CH3:22].O>CN(C=O)C>[CH2:21]([O:23][C:24](=[O:43])[CH2:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[C:29]([N:33]2[C:37]([NH:38][C:14]([NH:8][C:5]3[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=3)=[O:15])=[CH:36][C:35]([C:39]([CH3:42])([CH3:41])[CH3:40])=[N:34]2)[CH:28]=1)[CH3:22]

参加物

6

反応物 4

HCID 962WaterHCID 97314-FluoroanilineHCID 682631,1'-CarbonyldiimidazoleHCID 58842892ethyl 3-(3-(3-t-butyl-5-amino-1H-pyrazol-1-yl)phenyl)propanoate

生成物 1

HCID 588428503-(3-{3-t-Butyl5-[3-(4-fluoro-phenyl)-ureido]-pyrazol-1-yl}-phenyl)-propionic acid ethyl ester収率 33.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

A solution of 4-fluoro-phenylamine (111 mg, 1.0 mmol) and CDI (165 mg, 1.0 mmol) in DMF (2 mL) was stirred at RT for 30 min, and was then added to a solution of Example Z (315 mg, 1.0 mmol) in DMF (2 mL). The resulting mixture was stirred at RT overnight then added to water (50 mL). The reaction mixture was extracted with ethyl acetate (3×50 mL) and the combined organic extracts were washed with brine, dried (NaSO4) and filtered. After concentrated under reduced pressure, the residue was purified by flash chromatography to afford 3-(3-{3-t-butyl-5-[3-(4-fluoro-phenyl)-ureido]-pyrazol-1-yl}-phenyl)-propionic acid ethyl ester (150 mg, 33%). 1H-NMR (CDCl3): 7.91 (s, 1H), 7.42 (d, J=4.8 Hz, 1H), 7.37-7.34 (m, 2H), 7.28 (s, 1H), 7.17-7.16 (m, 2H), 6.98 (t, J=8.8 Hz, 2H), 6.59 (s, 1H), 4.04 (q, J=7.2 Hz, 2H), 3.03 (t, J=7.2 Hz, 2H), 2.77 (t, J=7.2 Hz, 2H), 1.36 (s, 9H), 1.17 (t, J=7.2 Hz, 3H); MS (ESI) m/z: 453 (M+H+).

後処理

  1. extractionThe reaction mixture was extracted with ethyl acetate (3×50 mL)
  2. washthe combined organic extracts were washed with brine
  3. dry with materialdried (NaSO4)
  4. filtrationfiltered
  5. concentrationAfter concentrated under reduced pressure
  6. customthe residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-f7d3ffa2491c407fa143b9eee8f6a3ca
出典データセット
uspto-grants-2010_06
特許番号
US07737283B2

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