تفاعل #834618

ord-b56d5ac36877430f9009941f76fb55aa

معادلة التفاعل

Cc1nccn1-c1nc(-c2ccc(Cl)cc2)c(CCCO)o1
4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol
CC1(C)CCC(C)(C)c2cc(O)ccc21
5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenol
CCCCP(CCCC)CCCC
tributylphosphine
O=C(N=NC(=O)N1CCCCC1)N1CCCCC1
1,1′-(azodicarbonyl)dipiperidine
Cc1nccn1-c1nc(-c2ccc(Cl)cc2)c(CCCOc2ccc3c(c2)C(C)(C)CCC3(C)C)o1
4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyloxy)propyl]oxazole

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزAfter the reaction mixture was concentrated

الإجراء التجريبي

To a mixture of 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol (318 mg), 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenol (409 mg), tributylphosphine (405 mg) and tetrahydrofuran (10 ml) was added 1,1′-(azodicarbonyl)dipiperidine (500 mg) at room temperature, and the resulting mixture was stirred for 1 hour. After the reaction mixture was concentrated, the residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyloxy)propyl]oxazole was obtained as a yellow oil (400 mg, 79%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07396848B1uspto-grants-2008_07