반응 #834604

ord-eb5daa47ce0d4366a986b61d32204da6

반응 방정식

Cc1nccn1-c1nc(-c2ccc(Cl)cc2)c(CCCO)o1
4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol
OC1Cc2ccccc2C1
2-hydroxyindane
CCCCP(CCCC)CCCC
tributylphosphine
O=C(N=NC(=O)N1CCCCC1)N1CCCCC1
1,1′-(azodicarbonyl)dipiperidine
Cc1nccn1-c1nc(-c2ccc(Cl)cc2)c(CCCOc2ccc3c(c2)CCC3)o1
4-(4-chlorophenyl)-5-[3-(5-indanyloxy)propyl]-2-(2-methyl-1-imidazolyl)oxazole

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축After the reaction mixture was concentrated

실험 절차

To a mixture of 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol (318 mg), 2-hydroxyindane (268 mg), tributylphosphine (405 mg) and tetrahydrofuran (10 ml) was added 1,1′-(azodicarbonyl)dipiperidine (400 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)-5-[3-(5-indanyloxy)propyl]-2-(2-methyl-1-imidazolyl)oxazole was obtained as an oil (418 mg, 96%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07396848B1uspto-grants-2008_07