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HRID 60134作成日:2026年10月24日

Perchloric Acid → 1-amino-4-(methoxycarbonyl)pyridin-2(1H)-iminium 2,4,6-trimethylbenzenesulfonate

https://huagongshe.com/ja/reaction/60134

反応式

関与物質

役割名称HCID仕込み量
反応物Perchloric AcidHCID 24247—
反応物Methyl 2-aminopyridine-4-carboxylateHCID 236984—
反応物ethyl (1E)-N-{[(2,4,6-trimethylphenyl)sulfonyl]oxy}ethanimidateHCID 5748625—
反応物2-AminoisonicotinateHCID 23171621—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒tert-Butyl methyl etherHCID 15413—
溶媒1,4-DioxaneHCID 31275—
生成物1-amino-4-(methoxycarbonyl)pyridin-2(1H)-iminium 2,4,6-trimethylbenzenesulfonateHCID 17849845988.6%

反応条件

温度3 °C

反応手順

70% Perchloric acid (18.9 ml) was added to a 1,4-dioxane (26 ml) solution of (Z)-ethyl N-(mesitylsulfonyl)oxyacetimidate (11.7 g) at 4° C. over 20 minutes. Thereafter, the reaction solution was stirred at 3° C. for 30 minutes, and it was then poured into water (100 ml). The precipitated solid was collected by filtration, and was then washed with water (45 ml) to obtain a white solid as a crude product. Methyl 2-aminoisonicotinate (5 g) was added to methylene chloride (35 ml), and the obtained mixture was then cooled to 3° C. The obtained crude product was dissolved in methylene chloride (40 ml), and only an organic layer was added to a methylene chloride solution of 2-aminoisonicotinate. The obtained mixture was stirred at 3° C. for 30 minutes. Thereafter, methyl tert-butyl ether (50 ml) was added to the reaction solution, and the precipitated solid was collected by filtration. The collected solid was washed with methyl tert-butyl ether (20 ml), and was then dried at 45° C., so as to obtain the title compound (10.7 g) in the form of a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440970B2
出典データセットuspto-grants-2016_09
ORD IDord-f2c2b502275b4457a2d77a9bb4faf6f8
出典メモuspto-grants-2016_09