تفاعل #40429

ord-a9b6035cb27d4c51a725621d2aa97cec

معادلة التفاعل

O=c1[nH]c2ccc(Cl)cc2c(=O)o1
5-chloroisatoic anhydride
Nc1ccc(Cl)cn1
2-amino-5-chloropyridine
C[Si](C)(C)[N-][Si](C)(C)C.[K+]
potassium bis(trimethylsilyl)amide
Cc1ccccc1
toluene
Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
(2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide
المردود 100.0%

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىdropwise at −78° C
  2. 2
    درجة الحرارةThe mixture was warmed up
  3. 3
    workup.STIRRINGstirred overnight
  4. 4
    أخرىAfter quenched by saturated ammonium chloride solution
  5. 5
    استخلاصthe mixture was extracted by ethyl acetate
  6. 6
    تجفيفThe organic layer was dried over magnesium sulfate
  7. 7
    تركيزconcentrated

الإجراء التجريبي

To a solution of 2-amino-5-chloropyridine (328 mg, 2.55 mmol) in tetrahydrofuran (5 ml) was 0.5M potassium bis(trimethylsilyl)amide in toluene (10 ml, 5.05 mmol) dropwise at −78° C. After stirred for additional 0.5 hr at −78° C., the mixture was added 5-chloroisatoic anhydride (0.5 g, 2.55 mmol) at −78° C. The mixture was warmed up to r.t gradually and stirred overnight. After quenched by saturated ammonium chloride solution, the mixture was extracted by ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide (0.71 g. 100%). MS found for C12H9Cl2N3O M+=282, (M+2)+=284.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07727981B2uspto-grants-2010_06