Ammonia → HCID 16100402, 화합물
반응식
[C:1]([CH2:3][C:4]1[CH:12]=[CH:11][C:7]2[O:8][CH2:9][O:10][C:6]=2[C:5]=1[CH2:13][C:14]#[N:15])#N.N>C(O)C.[Ni]>[O:10]1[C:6]2[C:5]3[CH2:13][CH2:14][NH:15][CH2:1][CH2:3][C:4]=3[CH:12]=[CH:11][C:7]=2[O:8][CH2:9]1참가 물질
5
실험 절차
(5-Cyanomethyl-1,3-benzodioxol-4-yl)acetonitrile (6.00 g, 30.0 mmoles) from Example 58C was reductively cyclized with Raney-Nickel (1.21 g) under a hydrogen atmosphere and high pressure (1100 p.s.i.) in a 10% ammonia in ethanol solution (121 mL) at 100° C. for one hour. The mixture was cooled, and the catalyst filtered off and washed with hot ethanol. The mixture was concentrated under reduced pressure, and the residue purified by normal phase HPLC on a Biotage pre-packed silica gel column eluting with 7:3 methylene chloride:methanol to afford the title compound. MS (DCI) m/z 192 (M+H)+.
후처리
- temperatureThe mixture was cooled
- filtrationthe catalyst filtered off
- washwashed with hot ethanol
- concentrationThe mixture was concentrated under reduced pressure
- customthe residue purified by normal phase HPLC on a Biotage pre-packed silica gel column
- washeluting with 7:3 methylene chloride
출처 및 근거
- ORD 기록
- ord-7d9a796838974b968ebe8ead506b1133
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09133145B2
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