Methanol → 3-(1,1-Dimethoxy-methyl)-6-[2-methoxy4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole

HRID 724415ノート

反応式

HRID 724415 の反応式
[CH3:1][O:2][CH:3]([C:6]1[C:14]2[C:9](=[CH:10][C:11](I)=[CH:12][CH:13]=2)[N:8]([CH2:16][O:17][CH2:18][CH2:19][Si:20]([CH3:23])([CH3:22])[CH3:21])[N:7]=1)[O:4][CH3:5].[CH3:24][O:25][C:26]1[CH:31]=[C:30]([O:32][CH:33]([Si](C)(C)C)[O:34][CH2:35][CH3:36])[CH:29]=[CH:28][C:27]=1B(O)O.C(=O)([O-])[O-].[Na+].[Na+].CO>C1C=CC=CC=1.CCOCC.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>[CH3:1][O:2][CH:3]([C:6]1[C:14]2[C:9](=[CH:10][C:11]([C:27]3[CH:28]=[CH:29][C:30]([O:32][CH2:33][O:34][CH2:35][CH2:36][Si:20]([CH3:22])([CH3:21])[CH3:19])=[CH:31][C:26]=3[O:25][CH3:24])=[CH:12][CH:13]=2)[N:8]([CH2:16][O:17][CH2:18][CH2:19][Si:20]([CH3:23])([CH3:22])[CH3:21])[N:7]=1)[O:4][CH3:5]

参加物

9

反応物 4

HCID 887MethanolHCID 10340Sodium CarbonateHCID 218772983-(1,1-dimethoxy-methyl)-6-iodo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazoleHCID 218774492-Methoxy4-(trimethylsilanyl-ethoxymethoxy)-phenylboronic acid

生成物 1

HCID 218774213-(1,1-Dimethoxy-methyl)-6-[2-methoxy4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole収率 164.4%

試薬・触媒・溶媒 4

HCID 178418397HCID 178418397、化合物触媒HCID 241Benzene溶媒HCID 962Water溶媒HCID 3283Diethyl Ether溶媒

実験手順

3-(1,1-Dimethoxy-methyl)-6-iodo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole (1.06 g, 2.37 mmol), 2-methoxy-4-(trimethylsilanyl-ethoxymethoxy)-phenylboronic acid (0.99 g, 3.32 mmol), and sodium carbonate (352 mg, 1.4 mmol) were stirred in a mixture of benzene (15 mL), MeOH (3 mL), and water (1 mL) in a flask purged with argon. Tetrakis(triphenylphosphine)palladium(0) (220 mg, 0.19 mmol) was added, and the reaction stirred at reflux for 16 h. The reaction was allowed to cool and was diluted with ether (70 mL). Organics were washed with H2O and brine (30 mL each), dried (Na2SO4), and concentrated in vacuo. Purification by silica gel chromatography (15% EtOAc/hexanes) gave 1.12 g (82%) of 3-(1,1-dimethoxy-methyl)-6-[2-methoxy-4-(2-trimethylsilanyl-ethoxymethoxy)-phenyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole as a faintly yellow oil. 1H NMR (300 MHz, CDCl3) δ 7.91 (d, 1H, J=8.4 Hz), 7.64 (s, 1H), 7.37 (dd, 1H, J=8.4, 1.2 Hz), 7.29 (d, 1H, J=8.4 Hz), 6.71–6.77 (m, 2H), 5.82 (s, 1H), 5.75 (s, 2H), 5.28 (s, 2H), 3.77–3.83 (m, 5H), 3.57 (t, 2H, J=8.4 Hz), 3.46 (s, 6H), 1.00 (t, 2H, J=8.4 Hz), 0.88 (t, 2H, J=8.4 Hz), 0.03 (s, 9H), −0.05 (s, 9H).

後処理

  1. custompurged with argon
  2. temperatureat reflux for 16 h
  3. temperatureto cool
  4. washOrganics were washed with H2O and brine (30 mL each)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. customPurification by silica gel chromatography (15% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-864934a05a12446eaf20107135964030
出典データセット
uspto-grants-2006_11
特許番号
US07141587B2

反応ノート

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