Water → 3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-(trifluoromethyl)benzenamine
반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[NH2:7][C:8]1[CH:9]=[C:10]([C:18]2[CH2:23][CH2:22][N:21]([C:24](OC(C)(C)C)=O)[CH2:20][CH:19]=2)[CH:11]=[C:12]([C:14]([F:17])([F:16])[F:15])[CH:13]=1.O.[OH-].[Na+]>C1COCC1>[CH3:24][N:21]1[CH2:20][CH:19]=[C:18]([C:10]2[CH:9]=[C:8]([NH2:7])[CH:13]=[C:12]([C:14]([F:15])([F:16])[F:17])[CH:11]=2)[CH2:23][CH2:22]1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Into a 100 mL round bottom flask was placed LAH (1.518 g, 40 mmol) and suspended in THF (30 mL). Flask placed into an ice bath. Tert-butyl 4-(3-amino-5-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate (1.368 g, 4 mmol) is added to THF (10 mL) and this solution is in turn added dropwise to the LAH suspension at 0° C. 15 min after addition was complete, flask is equipped with reflux condensor and allowed to reflux 15 h with stirring. Work up: Water (1.5 g) is added dropwise, then 15% NaOH(aq)(w/w)(1.5 g), followed by water (3 g). White precipitate forms after 20 h of stirring, filtered solids, removed solvent under reduced pressure. No further purification done. LC-MS (+) shows mass 257 (M+H), as expected for C13H15F3N2, mw 256.27.
후처리
- customInto a 100 mL round bottom flask was placed
- customFlask placed into an ice bath
- addition15 min after addition
- customflask is equipped
- temperaturewith reflux condensor
- temperatureto reflux 15 h
- stirringWhite precipitate forms after 20 h of stirring
- filtrationfiltered solids
- customremoved solvent under reduced pressure
- customNo further purification
출처 및 근거
- ORD 기록
- ord-c99e2c9b9c534901bfd73613baa6588f
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08178557B2
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