反応式
C(OCC1[C:15]2[C:10](=[CH:11][CH:12]=[C:13](C3C=CC=CC=3OC)[CH:14]=2)[NH:9]C(C)(C)C=1)C=C.Br[CH2:27][C:28]1[C:37]2[C:32](=[CH:33][CH:34]=[C:35]([C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][C:39]=3[O:44][CH3:45])[CH:36]=2)[NH:31][C:30]([CH3:47])([CH3:46])[CH:29]=1.C(O)C=C.C[Si]([N-][Si](C)(C)C)(C)C.[Na+]>C1COCC1>[CH3:45][O:44][C:39]1[CH:40]=[CH:41][CH:42]=[CH:43][C:38]=1[C:35]1[CH:36]=[C:37]2[C:32](=[CH:33][CH:34]=1)[NH:31][C:30]([CH3:47])([CH3:46])[CH:29]=[C:28]2[CH2:27][NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
4-Allyloxymethyl-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline 40 mg of 4-bromomethyl-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline, 44 μL of allyl alcohol, and 4 mL of 1 M solution of sodium bis(trimethylsilyl)amide in THF reacted to give 4.5 mg of the title compound as a foam.
出典と根拠
- ORDレコード
- ord-327afb34ff494ccc98e407e845ba3144
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06858627B2
関連ノート
読み込み中…