反応式
Cl[C:2]1[N:11]=[CH:10][C:9]2[C:4](=[N:5][CH:6]=[CH:7][N:8]=2)[N:3]=1.[H-].[Na+].C(=O)([O-])[O-].[K+].[K+].C(N(C(C)C)CC)(C)C>C(N(CC)CC)C>[N:3]1[C:4]2[C:9](=[N:8][CH:7]=[CH:6][N:5]=2)[CH:10]=[N:11][CH:2]=1参加物
6
実験手順
Treatment of chloro-pteridine V′ with nuclephile R7LY, in the presence of a base, such as sodium hydride, potassium carbonate, triethylamine, and diisopropylethylamine, and optionally using a catalyst such as Pd(0), affords Pteridine compound VI′. Suitable solvent for this reaction includes chloroform, methylene chloride, toluene, and tetrahydrofuran.
出典と根拠
- ORDレコード
- ord-d9c56d6283074992ae1b8b6cf1b5d281
- 出典データセット
- uspto-grants-2016_06
- 特許番号
- US09359361B2
関連ノート
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