反応式
CCCC[N+](CCCC)(CCCC)CCCC.[F-].[S:19]1[C:23]([C:24]([N:26]2[CH2:31][C:30]3([CH2:36][CH2:35][N:34]([CH2:37][C:38]4[CH:43]=[CH:42][CH:41]=[C:40]([CH2:44][CH2:45][O:46][Si](C(C)(C)C)(C)C)[C:39]=4[F:54])[CH2:33][CH2:32]3)[O:29][CH2:28][CH2:27]2)=[O:25])=[CH:22][C:21]2[CH:55]=[CH:56][CH:57]=[CH:58][C:20]1=2>C1COCC1>[S:19]1[C:23]([C:24]([N:26]2[CH2:31][C:30]3([CH2:36][CH2:35][N:34]([CH2:37][C:38]4[CH:43]=[CH:42][CH:41]=[C:40]([CH2:44][CH2:45][OH:46])[C:39]=4[F:54])[CH2:33][CH2:32]3)[O:29][CH2:28][CH2:27]2)=[O:25])=[CH:22][C:21]2[CH:55]=[CH:56][CH:57]=[CH:58][C:20]1=2参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
TBAF (1M solution in THF, 2 mL) was added to a solution of benzo[b]thiophen-2-yl(9-(3-(2-(tert-butyldimethylsilyloxy)ethyl)-2-fluorobenzyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanone (example 79, step a) (0.370 g) in THF (4 mL). After 0.5 h, the solution was concentrated. Purification by silica gel chromatography eluting with 10:1 ethyl acetate:triethylamine gave the subtitled compound as a gum. Yield 0.26 g.
後処理
- concentrationthe solution was concentrated
- customPurification by silica gel chromatography
- washeluting with 10:1 ethyl acetate
出典と根拠
- ORDレコード
- ord-565efb35d20f4f769ee3baeb56d8a9a9
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08629271B2
関連ノート
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