Diisopropylethylamine → 1-(1-Ethyl-propyl)-2-thiophen-2-ylmethyl-1H-benzoimidazole-5-carboxylic acid ((S)-1-cyanomethyl-3-methyl-butyl)-amide
反応式
[CH2:1]([CH:3]([N:6]1[C:10]2[CH:11]=[CH:12][C:13]([C:15]([OH:17])=O)=[CH:14][C:9]=2[N:8]=[C:7]1[CH2:18][C:19]1[S:20][CH:21]=[CH:22][CH:23]=1)[CH2:4][CH3:5])[CH3:2].C1C=NC2N(O)N=NC=2C=1.CCN(C(C)C)C(C)C.Cl.[NH2:44][C@@H:45]([CH2:49][CH:50]([CH3:52])[CH3:51])[CH2:46][C:47]#[N:48].S([O-])(O)(=O)=O.[Na+]>CN(C=O)C.O.C(Cl)CCl>[C:47]([CH2:46][C@@H:45]([NH:44][C:15]([C:13]1[CH:12]=[CH:11][C:10]2[N:6]([CH:3]([CH2:4][CH3:5])[CH2:1][CH3:2])[C:7]([CH2:18][C:19]3[S:20][CH:21]=[CH:22][CH:23]=3)=[N:8][C:9]=2[CH:14]=1)=[O:17])[CH2:49][CH:50]([CH3:52])[CH3:51])#[N:48]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 3
実験手順
To a solution of 4.93 g of 1-(1-ethyl-propyl)-2-thiophen-2-ylmethyl-1H-benzoimidazole-5-carboxylic acid in 50 ml of dry DMF 2.04 g of HOAT, 3.45 g of EDC and 4.35 ml of DIPEA were added at 0° C. After 30 min 3.29 g of (S)-3-Amino-5-methyl-hexanenitrile-hydrochloride and 4.35 ml of DIPEA were added and the reaction was stirred at rt for 4 h. The reaction was then poured into water and the pH was adjusted to 3 by the addition of 2 M aqueous sodium hydrogensulphate solution. The reaction was extracted with ethyl acetate three times. The combined organic phases were washed with saturated aqueous sodium bicarbonate solution and brine, dried over magnesium sulphate and concentrated. 5.90 g (90%) of 1-(1-Ethyl-propyl)-2-thiophen-2-ylmethyl-1H-benzoimidazole-5-carboxylic acid ((S)-1-cyanomethyl-3-methyl-butyl)-amide were obtained.
後処理
- extractionThe reaction was extracted with ethyl acetate three times
- washThe combined organic phases were washed with saturated aqueous sodium bicarbonate solution and brine
- dry with materialdried over magnesium sulphate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-5b1693a13d9a454196d244c133826784
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09156796B2
反応ノート
読み込み中…