関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dione | HCID 236270 | — |
| 反応物 | 8-Amino-5-[3,4-dichlorophenoxy]-6-methoxylepidine | HCID 609014 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 生成物 | 5-[3,4-Dichlorophenoxy]-6-methoxy-8-[4-phthalimido-1-methyl-butylamino]lepidine | HCID 633117 | — |
| 生成物 | 5-(3,4-Dichlorophenoxy)-6-methoxy-1methyl-8-[(4-phthalimido-1-methylbutyl)amino]quinoline | HCID 69464197 | — |
反応手順
A mixture of 12.4 g of 8-amino-5-(3,4-dichlorophenoxy)-6-methoxy-4-methylquinoline (36 mM) and 11.6 g of 4-oxo-1-phthalimidopentane (50 mM), in glacial acetic acid was stirred for 15 min under nitrogen and 2.6 g of sodium borohydride (70 mM) was added portionwise maintaining the temperature 25-35° C. After the addition, the reaction mixture was stirred for 30 min and then poured into ice cold solution of concentrated sodium hydroxide. The resulting precipitate was filtered and chromatographed over silica gel. Elution with hexanes:ethyl acetate 90:10 yielded the expected product of 5-(3,4-dichlorophenoxy)-6-methoxy-4-methyl-8-[(4-phthalimido-1-methylbutyl)amino]quino line which was crystallized from ether to give 12.4 g (22 mM) of yellow crystalline product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06376511B2 |
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| 出典データセット | uspto-grants-2002_04 |
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| ORD ID | ord-21095a23d393418fbcba0e1d862ca66b |
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| 出典メモ | uspto-grants-2002_04 |
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