Tetrahydrofuran → HCID 178440768, 화합물
반응식
[CH2:1]([N:3](CC)CC)C.[CH2:8]1[CH2:12]OC[CH2:9]1.[CH2:13]([C:17]1[CH:22]=[CH:21][C:20]([C:23]2[O:27][N:26]=[C:25]([C:28]3[CH:35]=[CH:34][C:31](C=O)=[CH:30][CH:29]=3)[N:24]=2)=[CH:19][CH:18]=1)[CH:14]([CH3:16])[CH3:15].C(O[BH-]([O:45][C:46](=[O:48])[CH3:47])OC(=O)C)(=O)C.[Na+].[C:50](O)(=O)C.[CH2:54]1[CH2:58]OC[CH2:55]1>CO>[C:54]([O:45][C:46]([C@H:47]1[CH2:12][C@@H:8]([NH:3][CH2:1][C:31]2[CH:34]=[CH:35][C:28]([C:25]3[N:24]=[C:23]([C:20]4[CH:19]=[CH:18][C:17]([CH2:13][CH:14]([CH3:15])[CH3:16])=[CH:22][CH:21]=4)[O:27][N:26]=3)=[CH:29][CH:30]=2)[CH2:9]1)=[O:48])([CH3:55])([CH3:58])[CH3:50]참가 물질
실험 절차
A solution of 3-cis-amino-cylcobutanecarboxylic acid tert-butyl ester (3.78 g, 19.6 mmol), triethylamine (4.0 mL, 29.4 mmol) and THF (100 mL) was added to a solution of 4-[5-(4-isobutyl-phenyl)-[1,2,4]oxadiazol-3-yl]-benzaldehyde (6.0 g, 19.6 mmol) in acetic acid/THF (1:10, 100 mL) and stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (8.06 g, 39.2 mmol) was added to the reaction mixture, stirred at room temperature for 12 hours, treated with methanol (50.0 mL) and concentrated in vacuo. The resulting residue was taken up in dichloromethane, washed sequentially with brine, saturated NaHCO3 and brine, dried (Na2SO4), filtered and concentrated in vacuo. Purification by flash chromatography (silica, 1:9-1:1 EtOAc:hexanes) provided the title compound (4.0 g, 44% yield) as a solid.
후처리
- stirringstirred at room temperature for 12 hours
- concentrationconcentrated in vacuo
- washwashed sequentially with brine, saturated NaHCO3 and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customPurification by flash chromatography (silica, 1:9-1:1 EtOAc:hexanes)
출처 및 근거
- ORD 기록
- ord-6d136bed5041475caa5d756bb0b224bd
- 출처 데이터셋
- uspto-grants-2010_03
- 특허 번호
- US07671043B2
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