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HRID 1784299作成日:2026年10月26日
Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate → Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate
https://huagongshe.com/reaction/1784299
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate | HCID 67235341 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethylacetate methanol | HCID 21584119 | — |
| 生成物 | Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate | HCID 11962077 | 83% |
反応手順
Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate (10.2 g) in solution in a mixture of ethyl acetate/methanol 3:1 (300 ml), and 10% palladium on carbon (1.02 g) are introduced into an autoclave. After stirring for 4 hours under a hydrogen atmosphere (3 bar) at a temperature of approximately 20° C., the catalyst is eliminated by filtration on celite and the filtrate is concentrated under reduced pressure at 40° C. in order to produce the expected compound in the form of an oil (7.75 g; 83% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07501525B2 |
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| 出典データセット | uspto-grants-2009_03 |
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| ORD ID | ord-738362d4b1254d849c6196150c37dc39 |
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| 出典メモ | uspto-grants-2009_03 |
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