Реакция #586291

ord-9ca14b91468345d188e30163013aaacb

Уравнение реакции

CCOCCO
2-ethoxyethanol
CCOC1(Cl)c2ccc(F)cc2N=CC1C#N
4-chloro-4-ethoxy-7-fluoro-3-quinolinecarbonitrile
Cn1ccnc1Sc1ccc(N)cc1Cl
3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamine
Cl.c1ccncc1
pyridine hydrochloride
CCOc1cc2c(Nc3ccc(Sc4nccn4C)c(Cl)c3)c(C#N)cnc2cc1F
4-({3-chloro-4-[(1-methyl-1H-imidazole-2-yl)sulfanyl]phenyl}amino)-6-ethoxy-7-fluoro-3-quinolinecarbonitrile

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Following the procedure of Example 1, a mixture of 2.4 g (9.72 mmol) 4-chloro-4-ethoxy-7-fluoro-3-quinolinecarbonitrile, 2.56 g (10.7 mmol) of 3-chloro-4-(1-methyl-1H-imidazole-2-ylsulfanyl)phenylamine and 1.2 g (10.38 mmol) of pyridine hydrochloride are refluxed in 2-ethoxyethanol (30 mL) at 110° C. for 1 hour to yield 4-({3-chloro-4-[(1-methyl-1H-imidazole-2-yl)sulfanyl]phenyl}amino)-6-ethoxy-7-fluoro-3-quinolinecarbonitrile as a pink solid, mp 251-254° C.

Источник

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