反応式
Br[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[NH2:10][C:11]([C:13]1[CH:14]=[C:15](B(O)O)[CH:16]=[CH:17][CH:18]=1)=[O:12].C(Cl)Cl.C([O-])([O-])=O.[Na+].[Na+].N#N>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].COCCOC>[CH:6]([C:5]1[CH:8]=[CH:9][C:2]([C:17]2[CH:16]=[CH:15][CH:14]=[C:13]([C:11]([NH2:10])=[O:12])[CH:18]=2)=[CH:3][CH:4]=1)=[O:7]参加物
8
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of 4-bromobenzaldehyde (2.78 g; 15.0 mmol), [3-(aminocarbonyl)-phenyl]boronic acid (2.72 g; 16.5 mmol), PdCl2(dppf).CH2Cl2 (0.306 g; 0.38 mmol), DME (25 mL) and Na2CO3 (25 mL of a 2M solution) was sparged 20 min with N2 and heated under reflux for 90 min (consumption of aryl bromide observed by LC/MS). Upon cooling, the mixture was partitioned between EtOAc/H2O, layers were separated, and the aqueous layer was extracted with EtOAc (×2). Combined organics were washed (H2O, brine), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (EtOAc/hexanes), affording the title compound as a tan solid. LC/MS (method A) 1.91 min, m/z 226 (M+H).
後処理
- temperatureheated
- temperatureunder reflux for 90 min
- custom(consumption of aryl bromide observed by LC/MS)
- temperatureUpon cooling
- customthe mixture was partitioned between EtOAc/H2O, layers
- customwere separated
- extractionthe aqueous layer was extracted with EtOAc (×2)
- washCombined organics were washed (H2O, brine)
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified by flash chromatography (EtOAc/hexanes)
出典と根拠
- ORDレコード
- ord-f16869d2600a431382fa4e227ab303ab
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822518B2
関連ノート
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