Potassium Hydroxide → 6-(Cyclopropylmethoxy)-5-(1-fluorocyclobutyl)pyridine-2-carboxylic acid
반응식
[OH-].[K+].Cl[C:4]1[N:9]=[C:8]([C:10]([OH:12])=[O:11])[CH:7]=[CH:6][C:5]=1[C:13]1([F:17])[CH2:16][CH2:15][CH2:14]1.[CH:18]1([CH2:21][OH:22])[CH2:20][CH2:19]1>CS(C)=O>[CH:18]1([CH2:21][O:22][C:4]2[N:9]=[C:8]([C:10]([OH:12])=[O:11])[CH:7]=[CH:6][C:5]=2[C:13]2([F:17])[CH2:16][CH2:15][CH2:14]2)[CH2:20][CH2:19]1참가 물질
실험 절차
Powdered potassium hydroxide (240 mg, 4.28 mmol) was added to a solution of 6-chloro-5-(1-fluorocyclobutyl)pyridine-2-carboxylic acid (Example 130 e, 393 mg, 1.71 mmol) in DMSO (7.86 mL). The mixture was stirred at ambient temperature for 15 minutes. Cyclopropylmethanol (136 mg, 153 μL, 1.88 mmol) was added and stirring was continued for 5 h at 60° C. Additional cyclopropylmethanol (68 mg, 76 μL, 94 mmol) was added, the mixture was stirred for 14 h at ambient temperature, poured onto ice/brine (100 mL) and extracted with TBME (2×100 mL). The aqueous layer was acidified with 1 N HCl and extracted with EtOAc (2×150 mL). The combined organic layers were washed with ice/brine (50 mL), dried over Na2SO4 and filtered. The solvent was removed under reduced pressure and the residue was purified by flash-chromatography (20 g SiO2, dichloromethane/MeOH 0-3% in 75 min) to give the title compound (65 mg, 31%) as colorless oil, MS (ESI) m/e=264.5 [M−H−].
후처리
- stirringstirring
- waitwas continued for 5 h at 60° C
- stirringthe mixture was stirred for 14 h at ambient temperature
- additionpoured onto ice/brine (100 mL)
- extractionextracted with TBME (2×100 mL)
- extractionextracted with EtOAc (2×150 mL)
- washThe combined organic layers were washed with ice/brine (50 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- customThe solvent was removed under reduced pressure
- customthe residue was purified by flash-chromatography (20 g SiO2, dichloromethane/MeOH 0-3% in 75 min)
출처 및 근거
- ORD 기록
- ord-849d1ba198ab4e878f1796c935b74993
- 출처 데이터셋
- uspto-grants-2016_04
- 특허 번호
- US09303012B2
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