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HRID 221559作成日:2026年10月26日

Ethyl 2-chloroethanecarboximidate hydrochloride → tert-butyl (2S)-2-[2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propylcarbamate

https://huagongshe.com/reaction/221559

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-chloroethanecarboximidate hydrochlorideHCID 12470659—
反応物tert-butyl (2S)-2-[(3-aminoquinolin-4-yl)amino]propylcarbamateHCID 86624121—
溶媒1,2-DichloroethaneHCID 11—
生成物tert-butyl (2S)-2-[2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propylcarbamateHCID 8662412346.6%

反応条件

温度60 °C

反応手順

tert-Butyl (2S)-2-[(3-aminoquinolin-4-yl)amino]propylcarbamate (4.60 g, 14.55 mmol) was dissolved in 150 mL of anhydrous 1,2-dichloroethane and the solution was stirred under N2. Ethyl 2-chloroethanimidoate hydrochloride (3.45 g, 21.8 mmol) was added and the reaction was heated to 60° C. for 24 hours. The reaction mixture was cooled and washed with saturated sodium bicarbonate solution (2×100 mL) followed by brine. The organic layer was dried over Na2SO4, filtered, and concentrated to give an orange solid. Chromatography (SiO2, 60-80% EtOAc/hexanes) gave tert-butyl (2S)-2-[2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propylcarbamate (2.54 g) as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207162B2
出典データセットuspto-grants-2012_06
ORD IDord-5181d69792a14636827cd7006264b6b2
出典メモuspto-grants-2012_06