تفاعل #63239

ord-407b8cae0d874901b9c8ba61bc41af52

معادلة التفاعل

Cl
HCl
COc1ccc(C(=O)O)c(OC(C)C)c1Br
3-bromo-4-methoxy-2-(1-methylethoxy)benzoic acid
O=C(n1ccnc1)n1ccnc1
1,1'-carbonyldiimidazole
CCN(CC)CC
triethylamine
Nc1nnn[nH]1
5-aminotetrazole
[Ca+2].[Cl-].[Cl-]
CaCl2
O=C(Nc1nnn[nH]1)c1ccccc1
N-1H-tetrazol-5-ylbenzamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةis warmed
  2. 2
    درجة الحرارةat reflux under nitrogen atmosphere
  3. 3
    درجة الحرارةThe resulting mixture is warmed
  4. 4
    درجة الحرارةat reflux for 30 hours
  5. 5
    ترشيحfiltered

الإجراء التجريبي

A mixture of 1.28 g (4.43 mmol) 3-bromo-4-methoxy-2-(1-methylethoxy)benzoic acid (prepared in Step 3) and 0.83 g 5.12 g (5.12 mmol) of 1,1'-carbonyldiimidazole in 15 ml of acetonitrile is warmed at reflux under nitrogen atmosphere (or CaCl2 filled drying tube) for one hour. The reaction mixture is treated with 1.07 g (10.62 mmol) of triethylamine and 0.44 g (5.17 mmol) of anhydrous 5-aminotetrazole. The resulting mixture is warmed at reflux for 30 hours. The reaction mixture is then poured onto 180 g of ice water and acidified with aqueous 10% HCl and filtered to give 1.32 g (1.58 theor., 84%) of 3-bromo-4-methoxy-2- 1-methylethoxy)-N-1H-tetrazol-5-ylbenzamide as a white solid having melting point 255°-256° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04764525uspto-grants-1988_08