8-(benzyloxy)-N-[(2R)-1-hydroxyhexan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide → 8-hydroxy-N-[(2R)-1-hydroxyhexan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide
反応式
C([O:8][C:9]1[C:10]2[N:11]([C:15]([C:19]([NH:21][C@H:22]([CH2:25][CH2:26][CH2:27][CH3:28])[CH2:23][OH:24])=[O:20])=[C:16]([CH3:18])[N:17]=2)[CH:12]=[CH:13][CH:14]=1)C1C=CC=CC=1.[H][H]>C(OCC)(=O)C.[Pd]>[OH:8][C:9]1[C:10]2[N:11]([C:15]([C:19]([NH:21][C@H:22]([CH2:25][CH2:26][CH2:27][CH3:28])[CH2:23][OH:24])=[O:20])=[C:16]([CH3:18])[N:17]=2)[CH:12]=[CH:13][CH:14]=1参加物
5
実験手順
350 mg of 10% palladium/carbon were added to a solution of 3.5 g (9.18 mmol) of 8-(benzyloxy)-N-[(2R)-1-hydroxyhexan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide in 250 ml of ethyl acetate, and hydrogen was applied at room temperature and atmospheric pressure. After 3 h, the mixture was filtered off through kieselguhr, the filter cake was washed intensively with ethyl acetate/methanol and the filtrate was evaporated to dryness. Methyl tert-butyl ether was added to the crude product obtained, the product was triturated and the solid was then filtered off and dried at 40° C. under high vacuum. This gave 2.1 g (79% of theory) of 8-hydroxy-N-[(2R)-1-hydroxyhexan-2-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide
後処理
- customwas applied at room temperature
- filtrationthe mixture was filtered off through kieselguhr
- washthe filter cake was washed intensively with ethyl acetate/methanol
- customthe filtrate was evaporated to dryness
- additionMethyl tert-butyl ether was added to the crude product
- customobtained
- customthe product was triturated
- filtrationthe solid was then filtered off
- customdried at 40° C. under high vacuum
出典と根拠
- ORDレコード
- ord-1d9d145e20964a1e812da492e4dd6844
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08778964B2
反応ノート
読み込み中…