تفاعل #1144

ord-2e59b47848294fe195989e641f0b30fb

معادلة التفاعل

Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCC#N)oc2c1
2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran
[N-]=[N+]=[N-].[Na+]
sodium azide
[Cl-].[NH4+]
ammonium chloride
CN(C)C=O
N,N-dimethylformamide
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCc3nnn[nH]3)oc2c1
5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole
المردود 78.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate
  2. 2
    غسيلAfter the ethyl acetate layer was washed with water
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    workup.DISTILLATIONthe solvent was distilled off
  5. 5
    غسيلFrom the fraction eluted with methanol-chloroform (5:95

الإجراء التجريبي

A mixture of 2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran (1.20 g), sodium azide (1.09 g), ammonium chloride (0.90 g) and N,N-dimethylformamide (30 ml) was stirred at 130° to 140° C. for 16 hours. The reaction mixture was poured over water and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with methanol-chloroform (5:95, v/v), 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole (1.05 g, 78%) was obtained, which was then recrystallized from dichloromethane-methanol to yield colorless prisms having a melting point of 177° to 178° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723479uspto-grants-1998_03