Piperidine → HCID 9968042、化合物
反応式
[C:1]1([C:7]2[N:8]=[C:9]([C:19](O)=[O:20])[N:10]([CH3:18])[C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:22][N:23]1[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1.[NH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1.C1CN([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C>C(Cl)Cl.O>[N:23]1([NH:22][C:19]([C:9]2[N:10]([CH3:18])[C:11]([C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[N:8]=2)=[O:20])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1.[N:29]1([C:19]([C:9]2[N:10]([CH3:18])[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[N:8]=2)=[O:20])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1参加物
実験手順
A mixture of 4,5-diphenyl-1-methylimidazole-2-carboxylic acid (50 mg, 0.18 mmol) from Step A, 1-aminopiperidine (0.052 mL, 0.36 mmol) (containing a small percent of piperidine as an impurity), PyBOP (NovaChem) (140 mg, 0.2 mmol) and N,N-diisopropyl-N-ethylamine (DIPEA) (0.065 mL, 0.2 mmol) in methylene chloride (2 mL) was stirred at rt for 20 hr. The reaction was diluted with water and extracted twice with methylene chloride. The organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified twice by prep TLC (1 mm, silica gel) eluting with 5% methylene chloride, 35% ethyl acetate in hexanes to afford the primary product N-(piperidin-1-yl)-4,5-diphenyl-1-methylimidazole-2-carboxamide and 2-(piperidin-1-ylcarbonyl)-4,5-diphenyl-1-methylimidazole as a byproduct.
後処理
- extractionextracted twice with methylene chloride
- washThe organic layers were washed with brine
- dry with materialdried over sodium sulfate
- customevaporated
- customThe residue was purified twice by prep TLC (1 mm, silica gel)
- washeluting with 5% methylene chloride, 35% ethyl acetate in hexanes
出典と根拠
- ORDレコード
- ord-b27f14d3b39a4580b05f9c485bc26cd9
- 出典データセット
- uspto-grants-2009_08
- 特許番号
- US07572785B2
反応ノート
読み込み中…