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HRID 2113479作成日:2026年10月27日
tert-butyl N'-(quinolin-2-yl)methylene-hydrazinecarboxylate → Tert-butyl N'-(quinolin-2-ylmethyl)-hydrazinecarboxylate
https://huagongshe.com/reaction/2113479
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | tert-butyl N'-(quinolin-2-yl)methylene-hydrazinecarboxylate | HCID 69201455 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Tert-butyl N'-(quinolin-2-ylmethyl)-hydrazinecarboxylate | HCID 69200678 | — |
反応手順
0.5 g 10% Pd/C are added to a solution of 15.00 g tert-butyl N′-(quinolin-2-yl)methylene-hydrazinecarboxylate in 200 ml of methanol. The resulting mixture is then shaken for 6 h at ambient temperature under 1 atm H2 pressure. Then the precipitate and the catalyst are separated from the solvent, the precipitate is dissolved in tetrahydrofuran, filtered again and in this way the catalyst is separated off. The THF solution is evaporated down and the residue is triturated with tert-butylmethylether, separated off and dried at 50° C. The tert-butylmethylether phase is evaporated down again and the residue is triturated this time with diethyl ether, separated off and dried at 50° C. The two solid fractions from the purification with tert-butylmethylether and diethyl ether are combined.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07432262B2 |
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| 出典データセット | uspto-grants-2008_10 |
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| ORD ID | ord-c58c2792fe6d4d1abb12e2f0d8cd9013 |
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| 出典メモ | uspto-grants-2008_10 |
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