تفاعل #355769

ord-138f7888e1f146aba0d8f346c4a2dd0b

معادلة التفاعل

O
water
CCn1c(C)nc(C)c1C(=O)C=CN(C)C
5-(3-Dimethylaminoprop-2-en-1-oyl)-1-ethyl-2,4-dimethylimidazole
N=C(N)Nc1ccccc1.O=C(O)O
phenylguanidine hydrogen carbonate
C[O-].[Na+]
sodium methoxide
CCn1c(C)nc(C)c1-c1ccnc(Nc2ccccc2)n1
title compound
المردود 70.0%
CCn1c(C)nc(C)c1-c1ccnc(Nc2ccccc2)n1
2-Anilino-4-(1-ethyl-2,4dimethylimidazol-5-yl)pyrimidine
المردود 70.0%

المذيبات

ظروف التفاعل

درجة الحرارة
150°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool to ambient temperature
  2. 2
    استخلاصThe solution was extracted EtOAc (2×50 ml)
  3. 3
    غسيلThe combined extracts were washed with water (2×50 ml)
  4. 4
    تجفيفbrine (2×50 ml), dried
  5. 5
    أخرىthe volatiles removed by evaporation
  6. 6
    أخرىThe residue purified by flash silica chromatography DCM

الإجراء التجريبي

5-(3-Dimethylaminoprop-2-en-1-oyl)-1-ethyl-2,4-dimethylimidazole (Method 10; 5.65 g, 25.6 mmol), phenylguanidine hydrogen carbonate (6.05, 30.7 mmol) and sodium methoxide (3.47 g, 64.2 mmol) were suspended in anhydrous DMA (80 ml) and the mixture heated at 150° C. for 18 hours. The reaction mixture was allowed to cool to ambient temperature and poured into water (50 ml). The solution was extracted EtOAc (2×50 ml). The combined extracts were washed with water (2×50 ml) and then brine (2×50 ml), dried and the volatiles removed by evaporation. The residue purified by flash silica chromatography DCM:MeOH (increasing in polarity from 100:0 to 96:4) to give the title compound (5.2 g, 70%) as an orange oil. NMR: 1.06 (t, 3H), 2.22 (s, 3H), 2.34 (s, 3H), 4.32 (q, 2H), 6.83 (d, 1H), 6.97 (t, 1H), 7.28 (t, 2H), 7.70 (d, 2H), 8.43 (d, 2H), 9.40 (s, 1H); m/z 294.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07446105B2uspto-grants-2008_11