تفاعل #429214

ord-a59bd4e12c2d4599a1dee1e3c3126397

معادلة التفاعل

CO
methanol
CC(=O)O
acetic acid
[C-]#N.[Na+]
sodium cyanide
COc1ccc(CSc2nc(-c3ccccc3)n(Cc3cc4c(cc3Cl)OCO4)c2C=O)cc1
product
COc1ccc(CSc2nc(-c3ccccc3)n(Cc3cc4c(cc3Cl)OCO4)c2C=O)cc1
1-((6-chloro-1,3-benzodioxol-5-yl) methyl)-4-(((4-methoxyphenyl) methyl) thio)-2-phenyl-1H-imidazole-5-carboxaldehyde
COC(=O)c1c(SCc2ccc(OC)cc2)nc(-c2ccccc2)n1Cc1cc2c(cc1Cl)OCO2
expected product
COC(=O)c1c(SCc2ccc(OC)cc2)nc(-c2ccccc2)n1Cc1cc2c(cc1Cl)OCO2
methyl 1-((6-chloro-1,3-benzodioxol-5-yl) methyl)-4-(((4-methoxyphenyl) methyl) thio)-2-phenyl-1H-imidazole-5-carboxylate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحby filtering
  2. 2
    غسيلwashing with ethyl acetate
  3. 3
    أخرىevaporating

الإجراء التجريبي

30 ml of methanol, 120 ul of acetic acid, 2.25 g of manganese oxide and 300 mg of sodium cyanide are added respectively to a solution of 600 mg of the product of Example 7 in methylene chloride. The reaction medium is left under agitation at ambient temperature for 96 hours, followed by filtering, washing with ethyl acetate and evaporating. 410 mg of expected product is obtained M.p.=158° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05856509uspto-grants-1999_01