関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Thiazoleacetic acid | HCID 236262 | — |
| 反応物 | 5,6-Diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil | HCID 11609665 | — |
| 生成物 | 3-[2-(4-Nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine | HCID 18449501 | — |
反応手順
By the method of Example 2, 4-thiazolylacetic acid is reacted with 5,6-diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil (6) to yield 3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine. By the method of Example 3, this substance is alkylated with a mixture of 1,2-dichloroethane, sodium carbonate and 2-(ethylamino)ethanol to yield 7-[2-ethyl(2-hydroxyethyl)amino]ethyl-3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(4-thiazolyl)methyl]xanthine. By the method of Example 4 this substance is reduced with hydrazine hydrate or hydrogen gas in the presence of a palladium catalyst to yield 3-[2-(4-aminophenyl)ethyl]-7-[2-ethyl(2-hydroxyethyl)amino]ethyl-1-propyl-8-[(4-thiazolyl)methyl]xanthine free base. The corresponding hydrochloride salt is then made on exposure to an excess of hydrogen chloride in solution.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07247639B2 |
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| 出典データセット | uspto-grants-2007_07 |
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| ORD ID | ord-89b2d692ba8e427bb8808a782009cd07 |
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| 出典メモ | uspto-grants-2007_07 |
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