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Sodium Carbonate → HCID 71469141、化合物

HRID 1500792
ノート
印刷プレビュー

反応式

HRID 1500792 の反応式
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][N:3]=1.[C:16]([NH:20][C:21]1[CH:22]=[C:23](B(O)O)[CH:24]=[CH:25][CH:26]=1)(=[O:19])[CH:17]=[CH2:18].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Cl:1][C:2]1[N:7]=[C:6]([C:23]2[CH:22]=[C:21]([NH:20][C:16](=[O:19])[CH:17]=[CH2:18])[CH:26]=[CH:25][CH:24]=2)[C:5]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][N:3]=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

7

反応物 4

HCID 10340Sodium CarbonateHCID 11776TriphenylphosphineHCID 103213313-Acrylamidophenylboronic acidHCID 57498061HCID 57498061、化合物

生成物 1

HCID 71469141HCID 71469141、化合物

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒
HCID 1140
Toluene
溶媒

反応条件

温度
90 °C

実験手順

2,4-Dichloro-N-phenylpyrimidin-5-amine (80 mg, 0.333 mmol), (3-acrylamidophenyl)-boronic acid (70.0 mg, 0.367 mmol), triphenylphosphine (3.50 mg, 0.013 mmol) and palladium acetate (1.496 mg, 6.66 μmol) were dissolved in toluene (8 mL) and 1M sodium carbonate (70.6 mg, 0.666 mmol). The reaction mixture was heated for 24 h at 90° C., allowed to cool to room temperature, and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate (20 mL) and washed with water (10 mL). The organic layer was separated, the aqueous layer was extracted with ethyl acetate (20 mL), the combined organic layers were washed with brine (20 mL), and dried over Na2SO4 and concentrated. The crude material was purified by flash chromatography (20% ethyl acetate/hexane) to the title compound. 1H NMR (400 MHz, CDCl3): δ 8.55 (s, 1H), 7.89 (s, 1H), 7.74 (s, 1H), 7.66 (d, 1H, J=8.4 Hz), 7.49 (d, 1H, J=8.0 Hz), 7.38 (t, 1H, J=8.0 Hz), 7.30 (m, 2H), 7.09-7.03 (m, 3H), 6.39 (m, 1H), 6.20 (m, 1H), 6.09 (dd, 1H, J=10.4 and 17.2 Hz), 5.75 (d, 1H, J=10.4 Hz); ESI-MS: 351.1 [M+H]+.

後処理

  1. temperatureto cool to room temperature
  2. customthe solvent was removed in vacuo
  3. dissolutionThe residue was dissolved in ethyl acetate (20 mL)
  4. washwashed with water (10 mL)
  5. customThe organic layer was separated
  6. extractionthe aqueous layer was extracted with ethyl acetate (20 mL)
  7. washthe combined organic layers were washed with brine (20 mL)
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated
  10. customThe crude material was purified by flash chromatography (20% ethyl acetate/hexane) to the title compound

出典と根拠

ORDレコード
ord-fd728284ae16451d9d46411915724a2f
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09206176B2

反応ノート

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