Cesium carbonate → Ammonia methanol

HRID 1163216ノート

反応式

HRID 1163216 の反応式
I[C:2]1[N:3]=[C:4]([CH:12]2[CH2:15][CH:14]([N:16]3[CH2:21][CH2:20][N:19]([CH3:22])[CH2:18][CH2:17]3)[CH2:13]2)[N:5]2[CH:10]=[CH:9][N:8]=[C:7]([NH2:11])[C:6]=12.[CH3:23][C:24]1[C:33]2[C:28](=[CH:29][C:30](B3OC(C)(C)[C:36](C)(C)[O:35]3)=[CH:31][CH:32]=2)[N:27]=[C:26]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[CH:25]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>COCCOC.O.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>[NH3:3].[CH3:36][OH:35].[CH3:23][C:24]1[C:33]2[C:28](=[CH:29][C:30]([C:2]3[N:3]=[C:4]([CH:12]4[CH2:15][CH:14]([N:16]5[CH2:21][CH2:20][N:19]([CH3:22])[CH2:18][CH2:17]5)[CH2:13]4)[N:5]4[CH:10]=[CH:9][N:8]=[C:7]([NH2:11])[C:6]=34)=[CH:31][CH:32]=2)[N:27]=[C:26]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[CH:25]=1

参加物

8

反応物 3

HCID 10796Cesium carbonateHCID 536290544-Methyl-2-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolineHCID 576810251-Iodo-3-[3-(4-methyl-piperazin-1-yl)-cyclobutyl]-imidazo[1,5-a]pyrazin-8-ylamine

生成物 2

HCID 21705897Ammonia methanolHCID 576809301-(4-Methyl-2-phenyl-quinolin-7-yl)-3-[3-(4-methyl-piperazin-1-yl)-cyclobutyl]-imidazo[1,5-a]pyrazin-8-ylamine

試薬・触媒・溶媒 3

HCID 178418397HCID 178418397、化合物触媒HCID 962Water溶媒HCID 80711,2-Dimethoxyethane溶媒

反応条件

温度
75 °C

実験手順

A mixture of 1-iodo-3-[3-(4-methyl-piperazin-1-yl)-cyclobutyl]-imidazo[1,5-a]pyrazin-8-ylamine (206 mg, 0.500 mmol) and 4-methyl-2-phenyl-7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-quinoline (190 mg, 0.550 mmol) and cesium carbonate (326 mg, 1.00 mmol) in 1,2-dimethoxyethane (10.0 mL) and water (2.0 mL) was evacuated and refilled with nitrogen (3×), then charged with tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.05 mmol), and the flask was again evacuated and refilled with nitrogen (3×). The mixture was heated at 75° C. overnight. The mixture was cooled to rt and diluted with ethyl acetate (30 mL), then washed with brine (115 mL); the organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated to afforded a yellow solid, which was purified by silica gel chromatography [CH2Cl2→5% MeOH/CH2Cl2→5% (2N NH3-MeOH)/CH2Cl2, then 10% (2N NH3-MeOH)/CH2Cl2 to give the title compound as a yellow solid; LC-MS (ES, Pos.): 504 [MH+]; 1H NMR (CDCl3, 400 MHz) δ 2.30 (s, 3H), 2.32-2.71 (m, 12H), 2.81 (d, J=0.9 Hz, 3H), 2.95 (m, 1H), 3.49 (m, 1H), 5.19 (brs, 2H), 7.11 (d, J=5.0 Hz, 1H), 7.19 (d, J=5.0 Hz, 1H), 7.45-7.55 (m, 3H), 7.75 (d, J=0.8 Hz, 1H), 7.94 (dd, J=8.6 Hz, 1.8 Hz, 1H), 8.12 (d, J=8.6 Hz, 1H), 8.16-8.19 (m, 2H), 8.39 (d, J=1.4 Hz, 1H).

後処理

  1. customwas evacuated
  2. additionrefilled with nitrogen (3×)
  3. customthe flask was again evacuated
  4. additionrefilled with nitrogen (3×)
  5. temperatureThe mixture was cooled to rt
  6. additiondiluted with ethyl acetate (30 mL)
  7. washwashed with brine (115 mL)
  8. dry with materialthe organic phase was dried over anhydrous sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customto afforded a yellow solid, which
  12. customwas purified by silica gel chromatography [CH2Cl2→5% MeOH/CH2Cl2→5% (2N NH3-MeOH)/CH2Cl2

出典と根拠

ORDレコード
ord-2d47ad977425449392ae7b2277db13ed
出典データセット
uspto-grants-2010_10
特許番号
US07820662B2

反応ノート

読み込み中…