Potassium Carbonate → 4-[4-(2,2-Difluoro-cyclopropylmethoxy)-phenyl]-piperidine hydrochloride
반응식
[F:1][C:2]1([F:11])[CH2:4][CH:3]1[CH2:5][O:6]S(C)(=O)=O.C(OC([N:19]1[CH2:24][CH2:23][CH:22]([C:25]2[CH:30]=[CH:29][C:28](O)=[CH:27][CH:26]=2)[CH2:21][CH2:20]1)=O)(C)(C)C.C([O-])([O-])=O.[K+].[K+].[Cl-:38].[Na+].O>CN(C=O)C>[ClH:38].[F:1][C:2]1([F:11])[CH2:4][CH:3]1[CH2:5][O:6][C:28]1[CH:27]=[CH:26][C:25]([CH:22]2[CH2:21][CH2:20][NH:19][CH2:24][CH2:23]2)=[CH:30][CH:29]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
4.48 g (19.2 mmol, 80%) Methanesulfonic acid 2,2-difluoro-cyclopropylmethyl ester are added to 5.93 g (19.2 mmol, 90%) 4-(4-hydroxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester and 5.36 g (38.5 mmol) K2CO3 in 60 mL DMF. Stirring is continued for 12 h at 50° C. under inert gas atmosphere. After that time, brine (50 mL) is added and the mixture is extracted with EtOAc (3×50 mL). The organic layer is separated, washed with brine, dried over sodium sulphate and the solvent is removed by evaporation. The residue is purified by column chromatography (silica gel; gradient PE:EtOAc 20:1→10:1). The residue is taken up in 20 mL DCM and 100 mL 4N HCl in EtOAc are added dropwise at 0° C. The mixture is stirred for 12 h at rt. After that time, the solvent is removed in vacuo to yield the desired product.
후처리
- extractionthe mixture is extracted with EtOAc (3×50 mL)
- customThe organic layer is separated
- washwashed with brine
- dry with materialdried over sodium sulphate
- customthe solvent is removed by evaporation
- customThe residue is purified by column chromatography (silica gel; gradient PE:EtOAc 20:1→10:1)
- addition100 mL 4N HCl in EtOAc are added dropwise at 0° C
- stirringThe mixture is stirred for 12 h at rt
- customAfter that time, the solvent is removed in vacuo
출처 및 근거
- ORD 기록
- ord-af5bca9b524d4374936ef868da62e6db
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765959B2
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