반응식
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[Si:25]([O:32][CH2:33][C@H:34]([CH3:56])[O:35][C:36]1[CH:37]=[C:38]([CH:42]=[C:43]([O:45][C:46]2[CH:51]=[CH:50][C:49]([S:52]([CH3:55])(=[O:54])=[O:53])=[CH:48][CH:47]=2)[CH:44]=1)[C:39](O)=[O:40])([C:28]([CH3:31])([CH3:30])[CH3:29])([CH3:27])[CH3:26].[NH2:57][C:58]1[S:59][CH:60]=[CH:61][N:62]=1>CN(C=O)C>[Si:25]([O:32][CH2:33][C@H:34]([CH3:56])[O:35][C:36]1[CH:37]=[C:38]([CH:42]=[C:43]([O:45][C:46]2[CH:47]=[CH:48][C:49]([S:52]([CH3:55])(=[O:53])=[O:54])=[CH:50][CH:51]=2)[CH:44]=1)[C:39]([NH:57][C:58]1[S:59][CH:60]=[CH:61][N:62]=1)=[O:40])([C:28]([CH3:31])([CH3:29])[CH3:30])([CH3:26])[CH3:27]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
HATU (513 mg, 1.35 mmol) was added to 3-((1S)-2-{[tert-Butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[4-(methylsulfonyl)phenoxy]benzoic acid (520 mg, 1.08 mmol) followed by addition of DMF (5 mL), disopropylethylamine (0.48 mL) and 2-aminothiazole (135 mg, 1.35 mmol) and the reaction was stirred under argon for 4 h. The solvent was evaporated and the residue was dissolved in saturated aqueous sodium hydrogencarbonate (30 mL) and ethyl acetate (50 mL). The organic layer was separated, washed with saturated aqueous ammonium chloride (30 mL) then dried (MgSO4), filtered and evaporated. Purification by column chromatography, eluting with 1:2 to 2:1 ethyl acetate:hexanes, afforded the title compound as a colourless oil (425 mg, 70%).
후처리
- customThe solvent was evaporated
- dissolutionthe residue was dissolved in saturated aqueous sodium hydrogencarbonate (30 mL)
- customThe organic layer was separated
- washwashed with saturated aqueous ammonium chloride (30 mL)
- dry with materialthen dried (MgSO4)
- filtrationfiltered
- customevaporated
- customPurification by column chromatography
- washeluting with 1:2 to 2:1 ethyl acetate
출처 및 근거
- ORD 기록
- ord-dd289d532c2d443f9197e77eb9b1b981
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07745475B2
연결된 노트
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