Acetic Acid → N-[4-({2-[(3-isopropylphenyl)amino]-1-methyl-1H-benzimidazol-5-yl}oxy)pyridin-2-yl]-2-(1-methylpiperidin-4-yl)acetamide
反応式
[CH:1]([C:4]1[CH:5]=[C:6]([NH:10][C:11]2[N:15]([CH3:16])[C:14]3[CH:17]=[CH:18][C:19]([O:21][C:22]4[CH:27]=[CH:26][N:25]=[C:24]([NH:28][C:29](=[O:37])[CH2:30][CH:31]5[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]5)[CH:23]=4)=[CH:20][C:13]=3[N:12]=2)[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2].[C:38](O)(=O)C.C=O.C([BH3-])#N.[Na+].C(=O)([O-])[O-].[Na+].[Na+]>O1CCCC1.CO>[CH:1]([C:4]1[CH:5]=[C:6]([NH:10][C:11]2[N:15]([CH3:16])[C:14]3[CH:17]=[CH:18][C:19]([O:21][C:22]4[CH:27]=[CH:26][N:25]=[C:24]([NH:28][C:29](=[O:37])[CH2:30][CH:31]5[CH2:32][CH2:33][N:34]([CH3:38])[CH2:35][CH2:36]5)[CH:23]=4)=[CH:20][C:13]=3[N:12]=2)[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2]参加物
7
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
To the mixture containing N-(4-(2-(3-isopropylphenylamino)-1-methyl-1H-benzo[d]imidazol-5-yloxy)pyridin-2-yl)-2-(piperidin-4-yl)acetamide (1 eq), glacial acetic acid (2 eq), and formaline (7.5 eq) in tetrahydrofuran:methanol (1:1) was added sodium cyanoborohydride (2 eq) and stirred at room temperature for one hour. Reaction neutralized with saturated sodium carbonate solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated to give crude product. Purification by HPLC to yield N-[4-({2-[(3-isopropylphenyl)amino]-1-methyl-1H-benzimidazol-5-yl}oxy)pyridin-2-yl]-2-(1-methylpiperidin-4-yl)acetamide. HPLC=3.51 min; MS: MH+=513.
後処理
- customReaction
- extractionextracted with ethyl acetate
- washThe organic layer was washed with brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customto give crude product
- customPurification by HPLC
出典と根拠
- ORDレコード
- ord-d034d5bc5a394e5480b48fd4fcafef94
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07423150B2
反応ノート
読み込み中…