Formaldehyde → tert-butyl 1-[2-(4-fluorophenyl)ethyl]-2-methyl-5-(1-methylpiperidin-4-yl)-1H-pyrrole-3-carboxylate
反応式
[C:1]([O:5][C:6]([C:8]1[CH:9]=[C:10]([CH:23]2[CH2:28][CH2:27][N:26]([C:29](OCC3C=CC=CC=3)=O)[CH2:25][CH2:24]2)[N:11]([CH2:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[C:12]=1[CH3:13])=[O:7])([CH3:4])([CH3:3])[CH3:2].C=O.[H][H]>CO.C(O)(=O)C.[Pd]>[F:22][C:19]1[CH:18]=[CH:17][C:16]([CH2:15][CH2:14][N:11]2[C:10]([CH:23]3[CH2:28][CH2:27][N:26]([CH3:29])[CH2:25][CH2:24]3)=[CH:9][C:8]([C:6]([O:5][C:1]([CH3:3])([CH3:2])[CH3:4])=[O:7])=[C:12]2[CH3:13])=[CH:21][CH:20]=1参加物
7
反応物 3
生成物 1
試薬・触媒・溶媒 3
実験手順
A 340 mg portion of benzyl 4-{4-(tert-butoxycarbonyl)-1-[2-(4-fluorophenyl)ethyl]-5-methyl-1H-pyrrol-2-yl}piperidine-1-carboxylate was dissolved in 7 ml of methanol, and 159 μl of 37% formalin, 3 drops of acetic acid and 45 mg of 10% palladium-activated carbon were added, followed by stirring at room temperature for 2 hours in an atmosphere of hydrogen. The reaction liquid was filtered through celite, the filtrate was concentrated under a reduced pressure, 50 ml of a saturated sodium bicarbonate aqueous solution was added to the residue, and the resulting solid was collected by filtration to obtain 232 mg of tert-butyl 1-[2-(4-fluorophenyl)ethyl]-2-methyl-5-(1-methylpiperidin-4-yl)-1H-pyrrole-3-carboxylate as a colorless solid.
後処理
- customThe reaction liquid
- filtrationwas filtered through celite
- concentrationthe filtrate was concentrated under a reduced pressure, 50 ml of a saturated sodium bicarbonate aqueous solution
- additionwas added to the residue
- filtrationthe resulting solid was collected by filtration
出典と根拠
- ORDレコード
- ord-c13ec720f4bc4c579080d45735ca7303
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08222274B2
反応ノート
読み込み中…