تفاعل #44712

ord-6909c9ea790740398f5e862b25298d5e

معادلة التفاعل

Nc1ccc(Oc2cccc3onc(N)c23)c(F)c1
4-(4-amino-2-fluorophenoxy)-1,2-benzisoxazole-3-amine
Nc1ccc(Oc2cccc3onc(N)c23)c(F)c1
4-(4-Amino-2-fluorophenoxy)-1,2-benzisoxazole-3-amine
Nc1nc(Cl)cc(Cl)n1
2-amino-4,6-dichloropyrimidine
Cl
hydrochloric acid
Nc1nc(Cl)cc(Nc2ccc(Oc3cccc4onc(N)c34)c(F)c2)n1
N-{4-[(3-Amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-(2-amino-6-chloro-4-pyrimidinyl)amine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture is heated
  2. 2
    درجة الحرارةat reflux overnight
  3. 3
    أخرىresulting in the formation of a colorless precipitate
  4. 4
    ترشيحThis is filtered off
  5. 5
    غسيلwashed repeatedly with water
  6. 6
    أخرىdried under high vacuum

الإجراء التجريبي

100 mg (0.39 mmol) of 4-(4-amino-2-fluorophenoxy)-1,2-benzisoxazole-3-amine (from example VII) and 63.3 mg (0.39 mmol) of 2-amino-4,6-dichloropyrimidine are suspended in 3 ml of water, and 0.04 ml of concentrated hydrochloric acid is added. The reaction mixture is heated at reflux overnight, resulting in the formation of a colorless precipitate. This is filtered off, washed repeatedly with water and dried under high vacuum.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07737153B2uspto-grants-2010_06