تفاعل #2075728

ord-08bd5b1fcffc4e73b644031b84d9fd1c

معادلة التفاعل

COc1c(Cl)nc(-c2ccc(Cl)c(OC)c2F)nc1Cl
4,6-Dichloro-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxy-pyrimidine
O
water
N
ammonia
COc1c(N)nc(-c2ccc(Cl)c(OC)c2F)nc1Cl
title compound
المردود 88.0%
COc1c(N)nc(-c2ccc(Cl)c(OC)c2F)nc1Cl
6-Chloro-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxypyrimidin-4-ylamine
المردود 88.0%

ظروف التفاعل

درجة الحرارة
125°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate thrice
  2. 2
    غسيلThe combined organic phases were washed once with brine
  3. 3
    أخرىdried
  4. 4
    أخرىevaporated

الإجراء التجريبي

4,6-Dichloro-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxy-pyrimidine (500 mg, 1.5 mmol) was suspended in ammonia saturated ethanol (10 mL) and heated in a CEM microwave at 125° C. for 30 min. The mixture was poured into 15 mL water and extracted with ethyl acetate thrice. The combined organic phases were washed once with brine, dried and evaporated to give the title compound (420 mg, 88% yield: 1H NMR (DMSO-d6) δ 7.59 (dd, 1H), 7.45 (br s, 2H), 7.39 (dd, 1H), 3.91 (s, 3H), 3.76 (s, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07642220B2uspto-grants-2010_01