Chlorotrimethylsilane → HCID 11604570、化合物
反応式
[CH3:1][N:2]([CH3:30])[C:3]1([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)[CH2:8][CH2:7][C:6](=[CH:9][C:10]([NH:12][CH2:13][CH2:14][C:15]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[NH:17][CH:16]=2)=[O:11])[CH2:5][CH2:4]1.[Cl:31][Si](C)(C)C>CC(CC)=O>[ClH:31].[CH3:30][N:2]([CH3:1])[C:3]1([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)[CH2:4][CH2:5][C:6](=[CH:9][C:10]([NH:12][CH2:13][CH2:14][C:15]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[NH:17][CH:16]=2)=[O:11])[CH2:7][CH2:8]1参加物
4
実験手順
2-(4-Dimethylamino-4-pyridin-2-ylcyclohexylidene)-N-[2-(1H-indol-3-yl)ethyl]acetamide (210 mg, 0.52 mmol) was dissolved in ethyl methyl ketone (5 ml), and chlorotrimethylsilane (0.19 ml, 1.5 mmol) was added. After 1.5 h the hydrochloride was isolated as a beige-coloured solid with an m.p. of 147-150° C. in a yield of 89% (203 mg).
出典と根拠
- ORDレコード
- ord-11ed6729b88f4fc28555802e1b1a7c98
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08017630B2
反応ノート
読み込み中…