تفاعل #2192308

ord-c773cfd7f8db4937b92ad816c6476972

معادلة التفاعل

c1ccc(Nc2nccc(-c3cnc4n3CCC4)n2)cc1
1,1-dimethoxy-4-dimethylaminobut-3-en-2-one
c1ccc(Nc2nccc(-c3cnc4n3CCC4)n2)cc1
2-Anilino-4-(6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl)pyrimidine
N=C(N)Nc1ccccc1.O=C(O)O
phenyl guanidine bicarbonate
CC(=O)N(C)C
dimethylacetamide
COC(OC)c1ccnc(Nc2ccccc2)n1
title compound
المردود 88.0%
COC(OC)c1ccnc(Nc2ccccc2)n1
2-Anilino-4-(dimethoxymethyl)pyrimidine
المردود 88.0%

ظروف التفاعل

درجة الحرارة
130°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool
  2. 2
    أخرىthe solvent removed by evaporation
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in EtOAc
  4. 4
    غسيلthe solution washed with water (×5), saturated sodium chloride (×2)
  5. 5
    أخرىdried
  6. 6
    أخرىevaporated

الإجراء التجريبي

A mixture of 1,1-dimethoxy-4-dimethylaminobut-3-en-2-one (Method 1; 20.0 g, 0.116 mol) and phenyl guanidine bicarbonate (25 g, 0.126 mol) in anhydrous dimethylacetamide (350 ml) was stirred and heated at 130° C. under nitrogen for 18 hours. The reaction mixture was allowed to cool and the solvent removed by evaporation. The residue was dissolved in EtOAc and the solution washed with water (×5), saturated sodium chloride (×2), dried and evaporated to give the title compound (24.7 g, 88%) as a dark brown oil. NMR: (CDCl3): 3.42 (s, 6H), 5.20 (s, 1H), 6.94 (d, 1H), 7.04 (t, 1H), 7.31 (m, 3H), 7.64 (d, 2H), 8.47 (d, 1H), m/z: 246.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07579344B2uspto-grants-2009_08