1-Butanaminium, N,N,N-tributyl-, fluoride, hydrate → HCID 69283084、化合物
反応式
O.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[C:20]([O:24][C:25](=[O:65])[CH2:26][N:27]1[C:35]2[C:30](=[CH:31][CH:32]=[C:33]([O:36][CH:37]([C:49]3[S:53][C:52]([C:54]4[CH:59]=[CH:58][C:57]([C:60]([F:63])([F:62])[F:61])=[CH:56][CH:55]=4)=[N:51][C:50]=3[CH3:64])[CH2:38][CH2:39][CH2:40][O:41][Si](C(C)(C)C)(C)C)[CH:34]=2)[CH:29]=[CH:28]1)([CH3:23])([CH3:22])[CH3:21]>O1CCCC1>[C:20]([O:24][C:25](=[O:65])[CH2:26][N:27]1[C:35]2[C:30](=[CH:31][CH:32]=[C:33]([O:36][CH:37]([C:49]3[S:53][C:52]([C:54]4[CH:59]=[CH:58][C:57]([C:60]([F:62])([F:63])[F:61])=[CH:56][CH:55]=4)=[N:51][C:50]=3[CH3:64])[CH2:38][CH2:39][CH2:40][OH:41])[CH:34]=2)[CH:29]=[CH:28]1)([CH3:22])([CH3:23])[CH3:21]参加物
4
実験手順
A 1 M solution of tetrabutylammonium fluoride hydrate (30 μl, 30 μmol) was added to an ice-cooled solution of [rac]-(6-[4-(tert-butyl-dimethyl-silanyloxy)-1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-butoxy}-indol-1-yl)-acetic acid tert-butyl ester (17 mg, 25 μmol) in tetrahydrofuran (0.5 ml). The ice bath was removed and the solution stirred for 30 min at ambient temperature. Ethyl acetate was added and the solution was washed with 1 N HCl. The aqueous layer was extracted with ethyl acetate and the combined extracts were washed two times with brine and dried over sodium sulfate. Evaporation of the solvent gave 14 mg (25 μmol, quant.) of the title compound as yellow oil.