Dimethylformamide → Methyl n-{4-[2-(4-chlorophenyl)-1-propylpent-4-en-1-yl]benzoyl}-beta-alaninate

HRID 2366343ノート

反応式

HRID 2366343 の反応式
[CH3:1][N:2]([CH:4]=[O:5])C.[ClH:6].NC[CH2:9][C:10]([O:12][CH3:13])=[O:11].CCN([CH:20]([CH3:22])[CH3:21])C(C)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)[C:34]2[CH:35]=[CH:36][CH:37]=[CH:38][C:33]=2N=N1>CCOC(C)=O>[Cl:6][C:33]1[CH:38]=[CH:37][C:36]([CH:35]([CH2:22][CH:20]=[CH2:21])[CH:34]([C:33]2[CH:38]=[CH:37][C:36]([C:4]([NH:2][CH2:1][CH2:9][C:10]([O:12][CH3:13])=[O:11])=[O:5])=[CH:35][CH:34]=2)[CH2:33][CH2:38][CH3:37])=[CH:35][CH:34]=1

参加物

6

実験手順

A DMF solution (20 ml) containing INTERMEDIATE 1 (1.66 g, 4.84 mmol), methyl β-alaninate hydrochloride (1.01 g, 7.26 mmol), DIEA (4.3 ml, 24.2 mmol) and BOP (3.21 g, 7.26 mmol) was stirred at room temperature for 1.5 hours. The solution was diluted with EtOAc and washed with water, brine and dried over Na2SO4. The filtered solution was concentrated and the residue purified by silica gel chromatography using a hexanes/EtOAc gradient to give the title compound. 1H NMR for the major diastereomer (500 MHz, CDCl3): δ 7.72 (d, J=8.2 Hz, 2H); 7.28 (d, J=8.3 Hz, 2H); 7.22 (d, J=8.2 Hz); 7.07 (d, J=8.4 Hz, 2H); 6.85-6.81 (m, 1H); 5.41-5.31 (m, 1H); 4.77-4.66 (m, 2H); 3.75-3.70 (m, 2H); 3.73 (s, 3H); 2.81-2.72 (m, 2H); 2.67 (t, J=5.9 Hz, 2H); 2.10-2.05 (m, 2H); 1.40-1.29 (m, 2H); 0.98-0.85 (m, 2H); 0.66 (t, J=7.3 Hz, 3H). LC1 4.03 min. (M+H)=428

後処理

  1. washwashed with water, brine
  2. dry with materialdried over Na2SO4
  3. concentrationThe filtered solution was concentrated
  4. customthe residue purified by silica gel chromatography

出典と根拠

ORDレコード
ord-9c4cc38f63414eeaa7e6ee20a736e4cc
出典データセット
uspto-grants-2014_04
特許番号
US08697740B2

反応ノート

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