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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

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N'-(quinolin-2-yl)methylene-hydrazinecarboxylateHCID 69201455—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物Tert-butyl N'-(quinolin-2-ylmethyl)-hydrazinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07432262B2
出典データセットuspto-grants-2008_10
ORD IDord-c58c2792fe6d4d1abb12e2f0d8cd9013
出典メモuspto-grants-2008_10