6-(4-Fluorophenyl)-4-phenoxypyrido[3,2-d]pyrimidine → 4-Ethoxy-6-(4-fluorophenyl)pyrido[3,2-d]pyrimidine
反応式
ClC1C2N=C(C3C=CC(F)=CC=3)C=CC=2N=CN=1.[O:19]([C:26]1[C:27]2[N:35]=[C:34]([C:36]3[CH:41]=[CH:40][C:39]([F:42])=[CH:38][CH:37]=3)[CH:33]=[CH:32][C:28]=2[N:29]=[CH:30][N:31]=1)[C:20]1C=CC=C[CH:21]=1>C(O)C>[CH2:20]([O:19][C:26]1[C:27]2[N:35]=[C:34]([C:36]3[CH:41]=[CH:40][C:39]([F:42])=[CH:38][CH:37]=3)[CH:33]=[CH:32][C:28]=2[N:29]=[CH:30][N:31]=1)[CH3:21]参加物
4
実験手順
This compound was synthesized from 4-chloro-6-(4-fluorophenyl)-pyrido[3,2-d]pyrimidine and ethanol in 87% yield, using the procedure described for the synthesis of 4-phenoxy-6-(4-fluorophenyl)-pyrido[3,2-d]pyrimidine. The mass spectrum characterising data was as follows: MS (m/z): 270 ([M+H]+, 100).
出典と根拠
- ORDレコード
- ord-146409fe420f4cffaac491b39cc161a4
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08232278B2
反応ノート
読み込み中…