反応式
[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+].[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[CH:23]=[CH:24][C:25]([C:28]([NH:30][CH2:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[O:29])=[N:26][CH:27]=2)=[C:18]([CH:38]=O)[CH:17]=1.[Cl:40][C:41]1[CH:46]=[CH:45][C:44]([C:47]2[CH:52]=[CH:51][C:50]([NH2:53])=[CH:49][CH:48]=2)=[CH:43][CH:42]=1.CC(O)=O>CCOC(C)=O.C1COCC1>[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[CH:23]=[CH:24][C:25]([C:28]([NH:30][CH2:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[O:29])=[N:26][CH:27]=2)=[C:18]([CH2:38][NH:53][C:50]2[CH:49]=[CH:48][C:47]([C:44]3[CH:45]=[CH:46][C:41]([Cl:40])=[CH:42][CH:43]=3)=[CH:52][CH:51]=2)[CH:17]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Solid NaBH(OAc)3 (110 mg, 0.52 mmol) was added to a THF solution (1.7 mL) of ethyl 3-(5-(4-chloro-2-formylphenyl)picolinamido)propanoate (125 mg, 0.35 mmol), 4′-chloro-[1,1′-biphenyl]-4-amine (106 mg, 0.52 mmol), and AcOH (0.02 mL, 0.35 mmol) and the resulting mixture was stirred at room temperature. After 16 h the resulting mixture diluted with EtOAc washed with water and brine, dried (Na2SO4), dry-packed onto silica gel and purified via column chromatography to yield the title compound.
後処理
- washwashed with water and brine
- dry with materialdried (Na2SO4)
- customdry-packed onto silica gel and purified via column chromatography
出典と根拠
- ORDレコード
- ord-722cbe1656444b1fa233e3a0f5126017
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08748624B2
関連ノート
読み込み中…