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HRID 27782作成日:2026年10月26日
2-Hydroxyquinoline → 5-(1-Hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyril
https://huagongshe.com/reaction/27782
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Hydroxyquinoline | HCID 6038 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 5-(1-Hydroxy-2-isopropylaminobutyl)-8-hydroxy-3,4-dihydrocarbostyril hydrochloride | HCID 23342111 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-(1-Hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyril | HCID 23342064 | — |
反応手順
3.28 g of 5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxy-3,4-dihydrocarbostyril hydrochloride was dissolved in 50 ml of methanol, and a 20% methanolic solution of sodium methylate was added to the solution in an amount of 2 moles per mole of the starting carbostyril compound. The mixture was then concentrated to dryness, and the residue was dissolved in dimethylformamide. 1.7 g of p-toluylic acid chloride was added to the solution while cooling with ice-water and the mixture was stirred for 4 hours at room temperature. The reaction mixture was poured into ice-water and extracted with chloroform. A mixture of diethyl ether and petroleum benzene was added to the chloroform extract to obtain 1.94 g of crystalline 5-(1-hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyril having a melting point of 151.5°-152.5° C. (after recrystallization from chloroform-n-hexane).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04223137 |
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| 出典データセット | uspto-grants-1980_09 |
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| ORD ID | ord-e1037e8dd75547f1aadf9b0d660bb31b |
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| 出典メモ | uspto-grants-1980_09 |
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