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HRID 521567作成日:2026年10月26日

(S)-(-)-N,alpha-Dimethylbenzylamine → (S)-methyl 3-methyl-6-(methyl (1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylate

https://huagongshe.com/reaction/521567

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-(-)-N,alpha-DimethylbenzylamineHCID 2060073—
反応物Methyl 6-chloro-3-methyl-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylateHCID 89287517—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-methyl 3-methyl-6-(methyl (1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylateHCID 7111599514.5%

反応条件

温度130 °C

反応手順

A mixture of compound methyl 6-chloro-3-methyl-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylate (2.0 g, 8.85 mmol) and (S)-N-methyl-1-phenylethanamine (2.39 g, 17.7 mmol) in anhydrous DMSO (20 mL) was stirred for 30 min at 130° C. under microwave condition. After cooled to room temperature, the mixture was diluted with EA (100 mL) and washed with H2O (100 mL*3). The organic layer was dried over Na2SO4, concentrated in vacuum and purified by flash column chromatography (silica-gel, DCM: MeOH=10:1) to give product (S)-methyl 3-methyl-6-(methyl (1-phenylethyl)amino)-[1,2,4]triazolo[4,3-b]pyridazine-8-carboxylate as a yellow oil (400 mg, 14.5%). LRMS (M+H+) m/z: calcd 326; found 326.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328117B2
出典データセットuspto-grants-2016_05
ORD IDord-a7b5c4f4c95f444e86c1cf4bcb686957
出典メモuspto-grants-2016_05