4,4-Difluoro-1′-(phenylmethyl)-1,4′-bipiperidine → 4,4-difluoro-1,4'-bipiperidine
反応式
C([N:8]1[CH2:13][CH2:12][CH:11]([N:14]2[CH2:19][CH2:18][C:17]([F:21])([F:20])[CH2:16][CH2:15]2)[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>CO.Cl.[Pd]>[F:21][C:17]1([F:20])[CH2:18][CH2:19][N:14]([CH:11]2[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)[CH2:15][CH2:16]1参加物
6
実験手順
A solution of 2.8 g (9.5 mmol) 1′-benzyl-4,4-difluoro-[1,4′]bipiperidinyl in 300 mL MeOH was hydrogenated in the presence of 1.2 g Pd/C (10%) at 50° C. and 50 psi hydrogen pressure with the addition of a few drops of 1 M HCl until the calculated volume of hydrogen had been taken up. The catalyst was filtered off and the filtrate was evaporated down under reduced pressure. The residue was triturated with diisopropylether, suction filtered and dried.
後処理
- filtrationThe catalyst was filtered off
- customthe filtrate was evaporated down under reduced pressure
- customThe residue was triturated with diisopropylether, suction
- filtrationfiltered
- customdried
出典と根拠
- ORDレコード
- ord-b9641564546c46fb8ebb21f5e72aff44
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700589B2
反応ノート
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