Bromotrimethylsilane → HCID 178485583、化合物
反応式
[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH:9]=[C:8]([C:10]2[N:15]=[C:14]([C:16](=[O:19])[NH:17][CH3:18])[C:13]([NH:20][C:21]3[C:26]([C:27]([F:30])([F:29])[F:28])=[CH:25][N:24]=[C:23]([NH:31][C:32]4[CH:46]=[CH:45][C:35]([CH2:36][CH2:37][CH2:38][CH2:39][PH:40](=[O:44])[O:41]CC)=[CH:34][C:33]=4[O:47][CH3:48])[N:22]=3)=[CH:12][CH:11]=2)[CH:7]=[N:6]1.Br[Si](C)(C)C>N1C=CC=CC=1>[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH:9]=[C:8]([C:10]2[N:15]=[C:14]([C:16](=[O:19])[NH:17][CH3:18])[C:13]([NH:20][C:21]3[C:26]([C:27]([F:29])([F:30])[F:28])=[CH:25][N:24]=[C:23]([NH:31][C:32]4[CH:46]=[CH:45][C:35]([CH2:36][CH2:37][CH2:38][CH2:39][PH:40](=[O:41])[OH:44])=[CH:34][C:33]=4[O:47][CH3:48])[N:22]=3)=[CH:12][CH:11]=2)[CH:7]=[N:6]1参加物
4
実験手順
A solution of ethyl (4-{[4-({6-[1-(3-hydroxypropyl)-1H-pyrazol-4-yl]-2-(methylcarbamoyl)pyridin-3-yl}amino)-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-methoxybenzyl)propylphosphinate (Compound 37B, 10 mg, 0.015 mmol) in pyridine (1 mL) was charged with bromotrimethylsilane (0.012 mL, 0.087 mmol). The reaction was stirred at rt for 20 min. The material was not isolated. MS (ESI): m/z 663.23 [M+H]+. UPLC: tR=0.85 min (polar—2 min).
後処理
- customThe material was not isolated
- customtR=0.85 min (polar—2 min)
出典と根拠
- ORDレコード
- ord-1564163956224e7d88eaccf279d71af0
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09133224B2
反応ノート
読み込み中…