Реакция #586290

ord-61a22bc46fd2421bac12684ef8617c6b

Уравнение реакции

N#Cc1cnc2cc(F)ccc2c1Cl
4-chloro-7-fluoro-3-quinolinecarbonitrile
Cn1ccnc1Sc1ccc(N)cc1Cl
3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamine
Cl.c1ccncc1
pyridine hydrochloride
Cn1ccnc1Sc1ccc(Nc2c(C#N)cnc3cc(F)ccc23)cc1Cl
4-({3-chloro-4-[(1-methyl-1H-imidazole-2-yl)thio]phenyl}amino)-7-fluoroquinoline-3-carbonitrile

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Following the procedure of Example 1, a mixture of 1.2 g (5.81 mmol) 4-chloro-7-fluoro-3-quinolinecarbonitrile, 1.53 g (6.39 mmol) of 3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamine and 0.671 g (5.81 mmol) of pyridine hydrochloride are refluxed in 2-ethoxyethanol (12 mL) at 120° C. for 45 minutes to yield 4-({3-chloro-4-[(1-methyl-1H-imidazole-2-yl)thio]phenyl}amino)-7-fluoroquinoline-3-carbonitrile as an off-white solid, mp 268-272° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07767671B2uspto-grants-2010_08