Cyanoacetic acid → 2-Cyano-N-(1-(4-(2-(diethylamino)ethoxy)phenyl)butyl)acetamide
反応式
[C:1]([CH2:3][C:4]([OH:6])=O)#[N:2].C1C=NC2N(O)N=NC=2C=1.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.C(N(C(C)C)CC)(C)C.[CH2:50]([N:52]([CH2:67][CH3:68])[CH2:53][CH2:54][O:55][C:56]1[CH:61]=[CH:60][C:59]([CH:62]([NH2:66])[CH2:63][CH2:64][CH3:65])=[CH:58][CH:57]=1)[CH3:51]>CN(C=O)C.C(OCC)(=O)C>[C:1]([CH2:3][C:4]([NH:66][CH:62]([C:59]1[CH:58]=[CH:57][C:56]([O:55][CH2:54][CH2:53][N:52]([CH2:67][CH3:68])[CH2:50][CH3:51])=[CH:61][CH:60]=1)[CH2:63][CH2:64][CH3:65])=[O:6])#[N:2]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To an ice cooled solution of cyanoacetic acid (37 mg, 0.43 mmol) in DMF (2 mL) was added 7-aza-1-hydroxybenzotriazole (HOAt; 59 mg, 0.43 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU; 165 mg, 0.43 mmol), diisopropylethylamine (DIPEA; 167 μL, 0.958 mmol) and 1-(4-(2-(diethylamino)ethoxy)phenyl)butan-1-amine (25; 115 mg, 0.43 mmol). The resulting mixture was then stirred at room temperature for 18 hours. The reaction mixture was diluted with ethyl acetate, washed with sat. aqueous NaHCO3 (2×) and sat. brine, dried over sodium sulfate, and concentrated to a thick yellow oil. Purification by flash silica gel column chromatography, eluting with 5:95 methanol/dichloromethane, afforded 29 (116 mg, 80%) as a yellow oil: MS (ES+) m/z 332.2 (M+H)+.
後処理
- washwashed with sat. aqueous NaHCO3 (2×) and sat. brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated to a thick yellow oil
- customPurification by flash silica gel column chromatography
- washeluting with 5:95 methanol/dichloromethane
出典と根拠
- ORDレコード
- ord-85628dcf14994fab9af901190173fd89
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08809377B2
反応ノート
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