HCID 13067091, 화합물 → HCID 13067111, 화합물
반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:14]#[N:15])=[CH:10][NH:11][C:12]=2[CH3:13])=[C:4]([C:16](=O)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[Cl:23])[CH:3]=1>[Ni].C(O)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3[C:9](=[CH:10][NH:11][C:12]=3[CH3:13])[CH2:14][N:15]=[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:4]=2[CH:3]=1참가 물질
실험 절차
A mixture of 8.5 g (24 mmol) of 4-[4-chloro-2-(2-chlorobenzoyl)phenyl]-5-methyl-1H-pyrrole-3-carbonitrile, 1 spoonful of Raney nickel and 250 ml of glacial acetic acid was hydrogenated on a Parr apparatus of 55 psi overnight. The catalyst was removed by filtration and the acetic acid was removed at reduced pressure. The residue was diluted with water, basififed with concentrated ammonium hydroxide and the resulting precipitate was collected by filtration. The precipitate was dissolved in tetrahydrofuran, dried over anhydrous sodium sulfate and concentrated at reduced pressure. The residue was crystallized from a mixture of ether and petroleum ether to give off-white cyrstals (mp 219°-222°). Recrystallization from a mixture of ether and methylene chloride gave colorless crystals, mp 221°-225°.
후처리
- customwas hydrogenated on a Parr apparatus of 55 psi overnight
- customThe catalyst was removed by filtration
- customthe acetic acid was removed at reduced pressure
- additionThe residue was diluted with water
- filtrationthe resulting precipitate was collected by filtration
- dissolutionThe precipitate was dissolved in tetrahydrofuran
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure
- customThe residue was crystallized from a mixture of ether and petroleum ether
- customto give off-white cyrstals (mp 219°-222°)
- customRecrystallization
- additionfrom a mixture of ether and methylene chloride
- customgave colorless crystals, mp 221°-225°
출처 및 근거
- ORD 기록
- ord-416a3fb2b1cf464d9bce4d7cb6d7c5bf
- 출처 데이터셋
- uspto-grants-1983_10
- 특허 번호
- US04409390
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