反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[NH:6][C:7]1[C:12](C(OCC)=O)=[CH:11][N:10]=[C:9]2[CH:18]=[N:19][NH:20][C:8]=12.[OH-].[Na+]>C(O)C>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]2[CH:18]=[N:19][NH:20][C:8]=12参加物
4
実験手順
Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate (0.600 g) was converted to the corresponding acid by heating under reflux with a 2% sodium hydroxide solution in ethanol (50 ml). The ethanol was removed under reduced pressure and the residue diluted with water (5 ml) and acidified to pH5 with dilute hydrochloric acid. The resulting acid was filtered off and dried, mp 255°-259° C.
後処理
- temperatureby heating
- customThe ethanol was removed under reduced pressure
- additionthe residue diluted with water (5 ml)
- filtrationThe resulting acid was filtered off
- customdried
出典と根拠
- ORDレコード
- ord-795da91dd8ec4d3bba0d28a4380803d5
- 出典データセット
- uspto-grants-1987_12
- 特許番号
- US04716160
関連ノート
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