Hydrochloric Acid → 2-(Difluoromethyl)-5-(isobutyramidomethyl)nicotinic acid
반응식
[F:1][CH:2]([F:21])[C:3]1[C:8]([C:9]([O:11]CC)=[O:10])=[CH:7][C:6]([CH2:14][NH:15][C:16](=[O:20])[CH:17]([CH3:19])[CH3:18])=[CH:5][N:4]=1.O.[OH-].[Li+].Cl>O1CCOCC1>[F:21][CH:2]([F:1])[C:3]1[C:8]([C:9]([OH:11])=[O:10])=[CH:7][C:6]([CH2:14][NH:15][C:16](=[O:20])[CH:17]([CH3:19])[CH3:18])=[CH:5][N:4]=1참가 물질
6
실험 절차
Dissolve ethyl 2-(difluoromethyl)-5-{[(2-methylpropanoyl)amino]methyl}pyridine-3-carboxylate (414 g, 1.38 mol, 1.0 equiv) in 1,4-dioxane (4.97 L). Add water (2.48 L) and lithium hydroxide (125.6 g, 2.96 mol, 2.5 equiv); then stir the resulting mixture for 60 min at room temperature. Concentrate the 1,4-dioxane solution to ½ volume under reduced pressure, and add hydrochloric acid (5 N, 1.16 L, 5.79 mol, 4.2 equiv) slowly to maintain temperature at less than 20° C. until the pH is 2. Collect the solids by filtration; air dry for 18 hours; and then in a vacuum oven at 40° C. for 18 hours to give a white solid, (355.4 g, 94.7% yield). MS (m/z) 303 (M+1).
후처리
- concentrationConcentrate the 1,4-dioxane solution
- temperatureto maintain temperature at less than 20° C. until the pH is 2
- customCollect the solids
- filtrationby filtration
- customair dry for 18 hours
- customand then in a vacuum oven at 40° C. for 18 hours to give a white solid, (355.4 g, 94.7% yield)
출처 및 근거
- ORD 기록
- ord-f84b6cf067d94450a290f699b2478cc6
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08648200B2
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