반응 #9518
ord-a616420e3c0545a6852c5145c960a6c0
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반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1온도The reaction was heated
- 2온도at reflux for 14 hours
- 3기타The crude product was recrystallized from methanol
- 4기타purified by column chromatography on silica gel (
- 5세척eluting with chloroform
- 6기타The solid was then purified by HPFC
실험 절차
Dimethyl 4-(4-amino-7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)butane-1-sulfonamide (0.66 g, 1.4 mmol) and phenyl boronic acid (0.20 g, 1.6 mmol) were coupled according to the method described in Part J of Example 1. The reaction was heated at reflux for 14 hours, and the work-up procedure used in Part F of Examples 125–135 was followed. The crude product was recrystallized from methanol and then purified by column chromatography on silica gel (eluting with chloroform:CMA in a gradient from 100:0 to 90:10). The solid was then purified by HPFC to provide 0.14 g of dimethyl 4-[4-amino-2-ethoxymethyl-7-phenyl-1H-imidazo[4,5-c]quinolin-1-yl]butane-1-sulfonamide as Off-white needles, mp 207–208° C.