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HRID 431600생성일: 2026년 10월 25일

Dichloromethane → tert-butyl 2-[2-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate

https://huagongshe.com/reaction/431600

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참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Ammonium HydroxideHCID 14923—
반응물tert-butyl 2-[2-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamateHCID 21898031—
용매1,2-DichloroethaneHCID 11—
생성물tert-butyl 2-[2-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamateHCID 21898017—

반응 단계

A solution of tert-butyl 2-[2-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (3.68 g, 8.60 mmol) in 100 mL of 1,2-dichloroethane was heated to 80° C. and treated with 10 mL of concentrated NH4OH solution. To the rapidly stirred solution was added solid p-toluenesulfonyl chloride (1.87 g, 9.81 mmol) over a 10 min. period. The reaction mixture was then sealed in a pressure vessel and heating was continued for 2 h. The reaction mixture was then cooled and treated with 100 mL of CH2Cl2. The reaction mixture was then washed with H2O, 1% Na2CO3 solution (3×) and brine. The organic portion was dried over Na2SO4 and concentrated to give 3.68 g of tert-butyl 2-[2-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate as a light brown foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660747B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-999c6ac3a7be4d3da225b95bd829b8b0
출처 메모uspto-grants-2003_12