HCID 58149918、化合物 → HCID 58149902、化合物
反応式
Br[Zn][CH2:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7].Br[C:12]1[C:21]2[CH:20]=[CH:19][CH:18]=[C:17]([C:22]#[N:23])[C:16]=2[CH:15]=[CH:14][N:13]=1>C1COCC1.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>[C:22]([C:17]1[CH:18]=[CH:19][CH:20]=[C:21]2[C:16]=1[CH:15]=[CH:14][N:13]=[C:12]2[CH2:3][CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])#[N:23]参加物
実験手順
Bromo[4-(ethyloxy)-4-oxobutyl]zinc (0.5 M in THF, 26 ml) was added dropwise to a solution of 1-bromo-5-isoquinolinecarbonitrile (D38; 1 g) and tetrakis(triphenylphosphine)palladium(0) (20 mg) in THF (5 ml). The resulting solution was heated to reflux for 3 hours. The solvent was evaporated in vacuo and the residue was dissolved in DCM (50 ml). The organic solution was washed with 0.5 M aq. NaOH (15 ml), followed by washing with water and brine. The organic phase was dried over anhydrous sodium sulphate. The dried solution was filtered and the filtrate was concentrated. The residue was purified by column chromatography to give the title compound (0.65 g). δH (CDCl3, 400 MHz): 1.28 (3H, t), 2.20 (2H, m), 2.50 (2H, m), 3.41 (2H, m), 4.16 (2H, q), 7.71 (1H, dd), 7.93 (1H, d), 8.12 (1H, dd), 8.54 (1H, d), 8.63 (1H, d). MS (ES): C16H16N2O2 requires 268. found 269.1 (M+H+).
後処理
- temperatureThe resulting solution was heated
- temperatureto reflux for 3 hours
- customThe solvent was evaporated in vacuo
- dissolutionthe residue was dissolved in DCM (50 ml)
- washThe organic solution was washed with 0.5 M aq. NaOH (15 ml)
- washby washing with water and brine
- dry with materialThe organic phase was dried over anhydrous sodium sulphate
- filtrationThe dried solution was filtered
- concentrationthe filtrate was concentrated
- customThe residue was purified by column chromatography
出典と根拠
- ORDレコード
- ord-358e93d8f00c423d9ea963fd52ca2ee9
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08329730B2
反応ノート
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