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HRID 40212作成日:2026年10月25日
3-Hydrazinyl-6-phenylpyridazine → 3-Methoxy-6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline
https://huagongshe.com/reaction/40212
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Hydrazinyl-6-phenylpyridazine | HCID 6409842 | — |
| 反応物 | Tert-butyl 2-(3-methoxyquinolin-6-yl)acetate | HCID 59843087 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 生成物 | 3-Methoxy-6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline | HCID 57691355 | — |
反応手順
A mixture of tert-butyl 2-(3-methoxyquinolin-6-yl)acetate (148 mg) and 1-(6-phenylpyridazin-3-yl)hydrazine (126 mg) in HCl (conc., 0.3 mL) was heated at 100° C. for 5 min and was subject to microwave heating (180° C., 15 min) The yellow sludge was quenched with NaOH (5N, 1 mL). The pink mixture was filtered and washed with NaOH (1 N, 1 mL), H2O (2 mL). The solid was suspended in DMF (2 mL)-DCM (2 mL). MeI (0.2 mL) was added followed by the addition of NaOH (2N, 1 mL). After 2 h, the mixture was partitioned between DCM (10 mL) and aqueous Na2SO3 (5 mL). The organic was dried over MgSO4, concentrated, and purified in silica (1-15% MeOH in DCM) to give the product as a yellow powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524900B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-ac00229e44b74023bf42debc5b683c56 |
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| 出典メモ | uspto-grants-2013_09 |
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