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HRID 1084834作成日:2026年10月25日
Dimethylformamide → 1-[3-(3-dimethylamino-2-methylpropoxy)phenyl]-3-phenyl-1H-pyrazolo[3,4-b]pyridine.maleate
https://huagongshe.com/reaction/1084834
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-Chloro-2-methylpropyl(dimethyl)amine | HCID 90906 | — |
| 反応物 | 1-(3-hydroxyphenyl)-3-phenyl-1H-pyrazolo[3,4-b]pyridine | HCID 14796252 | — |
| 生成物 | 1-[3-(3-dimethylamino-2-methylpropoxy)phenyl]-3-phenyl-1H-pyrazolo[3,4-b]pyridine.maleate | HCID 86744715 | — |
反応手順
In 70 ml of dimethylformamide were suspended 4.0 g of 1-(3-hydroxyphenyl)-3-phenyl-1H-pyrazolo[3,4-b]pyridine, 2.6 g of 3-dimethylamino-2-methylpropylchloride and 2.3 g of potassium carbonate. The mixture was stirred at 100° C. for 6 hours. The solvent was distilled off under reduced pressure. By adding maleic acid, the residue was converted into the salt. The obtained crude crystals were recrystallized from a mixed solvent of ethyl acetate and ethanol to give 5.2 g of 1-[3-(3-dimethylamino-2-methylpropoxy)phenyl]-3-phenyl-1H-pyrazolo[3,4-b]pyridine·maleate, m.p. 134°-136° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05006520 |
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| 出典データセット | uspto-grants-1991_04 |
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| ORD ID | ord-237e117d73634362be1ff1f2c2c80e6d |
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| 出典メモ | uspto-grants-1991_04 |
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