反応式
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1I.CC1(C)C(C)(C)OB([C:18]2[CH:23]=[CH:22][C:21]([CH:24]3[CH2:29][CH2:28][N:27]([CH2:30][C:31]([F:34])([F:33])[F:32])[CH2:26][CH2:25]3)=[CH:20][CH:19]=2)O1.C(=O)([O-])[O-].[Na+].[Na+]>C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl.CC#N>[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[C:18]1[CH:19]=[CH:20][C:21]([CH:24]2[CH2:25][CH2:26][N:27]([CH2:30][C:31]([F:34])([F:32])[F:33])[CH2:28][CH2:29]2)=[CH:22][CH:23]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of 2-bromo-1-iodo-4-methylbenzene (0.764 g, 2.57 mmol), the title compound from Example 60 Step B (1.00 g, 2.71 mmol), dichloro bis(triphenylphosphine)palladium(II) (0.095 g, 0.135 mmol), sodium carbonate (5.42 mL of 1 M solution, 5.42 mmol) and MeCN (5.42 mL) was heated at 110° C. overnight. Organic layer was separated. Aqueous layer was extracted with hexanes-EtOAc. The organic layers were combined and concentrated. Silica gel flash chromatography eluting with hexanes:EtOAc (20:1 to 9:1 v/v) gave the title compound: LCMS m/z 414.0 [M+H+]; 1H NMR (500 MHz, CDCl3) δ 7.54 (s, 1 H),7.40 (d, J=8.1 Hz, 2 H), 7.31 (d, J=8.1 Hz, 2 H),7.26 (d, J=7.8 Hz, 1 H),7.20 (d, J=7.8 Hz, 1 H),3.16 (m, 2 H), 3.08 (q, J=9.8 Hz, 2 H),2.57 (m, 3 H),2.42 (s, 3 H).1.95-1.88 (m, 4 H).
後処理
- customOrganic layer was separated
- extractionAqueous layer was extracted with hexanes-EtOAc
- concentrationconcentrated
- washSilica gel flash chromatography eluting with hexanes:EtOAc (20:1 to 9:1 v/v)
出典と根拠
- ORDレコード
- ord-730c1701cb624e3c919fef31c05fc710
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08895583B2
関連ノート
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