تفاعل #1810843

ord-60c7763639cb432c8278fad5165a8f4d

معادلة التفاعل

O
water
Cc1ncc(C(=O)C=CN(C)C)n1C1CCC1
5-(3-Dimethylaminoprop-2-en-1-oyl)-1-cyclobutyl-2-methylimidazole
Cc1ncc(C(=O)C=CN(C)C)n1C1CCC1
5-(3-Dimethylaminoprop-2-enoyl)-1-cyclobutyl-2-methylimidazole
N=C(N)Nc1ccccc1.O=C(O)O
phenylguanidine hydrogen carbonate
C[O-].[Na+]
sodium methoxide
Cc1ncc(-c2ccnc(Nc3ccccc3)n2)n1C1CCC1
title compound
المردود 35.0%
Cc1ncc(-c2ccnc(Nc3ccccc3)n2)n1C1CCC1
2-Anilino-4-(1-cyclobutyl-2-methylimidazol-5-yl)pyrimidine
المردود 35.0%

المذيبات

ظروف التفاعل

درجة الحرارة
160°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 was triturated with ether
  7. 7
    ترشيحcollected by filtration and air
  8. 8
    أخرىdried

الإجراء التجريبي

5-(3-Dimethylaminoprop-2-en-1-oyl)-1-cyclobutyl-2-methylimidazole (Method 37; 466 mg, 2 mmol), phenylguanidine hydrogen carbonate (434 g, 2.2 mmol) and sodium methoxide (238 mg, 4.4 mmol) were suspended in anhydrous DMA (5 ml) and the mixture heated at 160° C. for 3 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 was triturated with ether, collected by filtration and air dried to give the title compound (205 mg, 35%) as a brown solid. NMR: 1.63 (m, 2H), 2.35 (m, 4H), 2.53 (s, 3H), 5.5 (m, 1H), 6.96 (d, 2H), 7.28 (m, 4H), 7.70 (d, 2H), 8.39 (d, 1H), 9/45 (s, 1H); m/z 306.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07485638B2uspto-grants-2009_02