反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH:9]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:10]([C:20](=O)[CH:21]([CH3:23])[CH3:22])[C:11]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:12])=[CH:4][CH:3]=1.[NH2:32][CH2:33][CH2:34][CH:35]([O:39][CH2:40][CH3:41])[O:36][CH2:37][CH3:38].C(O)(=O)C(C)(C)C>C1(C)C=CC=CC=1>[CH2:37]([O:36][CH:35]([O:39][CH2:40][CH3:41])[CH2:34][CH2:33][N:32]1[C:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)=[C:9]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:10]([C:11]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:12])=[C:20]1[CH:21]([CH3:22])[CH3:23])[CH3:38]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 22.5 °C
実験手順
To a nitrogen purged flask equipped with a mechanical stirrer is added 130 kg (311 mol) of (±)4-fluoro-α-[2-methyl-1-oxopropyl]-γ-oxo-N,β-diphenylbenzenebutaneamide mixture of [R-(R*,R*)], [R-(R*,S*)], [S-(R*,R*)] and [S-(R*,S*)] isomers, 540 L of heptanes and 60 L of toluene, 59 kg (400 mol) of 3-amino-1,1-diethoxypropane, and 22.3 kg (218 mol) of pivalic acid. The mixture is stirred and heated to reflux, removing water with a Dean Stark trap. The mixture is refluxed 32 hours and slowly cooled to 60°-65° C., diluted with 500 L of 2-propanol-water (3:2), seeded, and cooled to 20-25° C. The product is isolated by filtration, washed with 300 L of 2-propanol, and dried in vacuo to yield 133.5 kg of 1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1 H-pyrrole-3-carboxamide; mp 125.1°-127.7° C. after recrystallization from ethanol.
後処理
- customTo a nitrogen purged flask equipped with a mechanical stirrer
- additionis added
- temperatureheated
- temperatureto reflux
- customremoving water with a Dean Stark trap
- temperatureThe mixture is refluxed 32 hours
- temperatureslowly cooled to 60°-65° C.
- additiondiluted with 500 L of 2-propanol-water (3:2)
- customThe product is isolated by filtration
- washwashed with 300 L of 2-propanol
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-bc325b8893574d99b132a5fdc2ef0766
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05245047
関連ノート
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