تفاعل #302878

ord-927182cec925424f8410152396a87b1f

معادلة التفاعل

Cc1cc(=O)nc(N)[nH]1
6-methylisocytosine
C=C(C)C(=O)OCCN=C=O
2-isocyanatoethyl methacrylate
CCC[CH2][Sn](=[O])[CH2]CCC
dibutyltin oxide
CC=CC(=O)OCCNC(=O)Nc1nc(=O)cc(C)[nH]1
3-methyl-2-propenoic acid-2-[[[(1,4-dihydro-6-methyl-4-oxo-2-pyrimidinyl)amino]carbonyl]amino]ethyl ester

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITION100 mg BHT was added
  2. 2
    ترشيحThe mixture was filtered at 90° C
  3. 3
    درجة الحرارةUpon cooling down to room temperature 2-methyl-2-propenoic acid-2-[[[(1,4-dihydro-6-methyl-4-oxo-2-pyrimidinyl)amino]carbonyl]amino]ethyl ester
  4. 4
    أخرىto crystallize
  5. 5
    workup.ADDITION500 ml acetone was added

الإجراء التجريبي

37.5 g (0.3 mol) 6-methylisocytosine, 55.8 g (0.36 mol) 2-isocyanatoethyl methacrylate and 3.7 g (0.015 mmol) dibutyltin oxide were added to 400 ml dimethylacetamide. 100 mg BHT was added and the mixture was heated to 90° C. for one hour. The mixture was filtered at 90° C. Upon cooling down to room temperature 2-methyl-2-propenoic acid-2-[[[(1,4-dihydro-6-methyl-4-oxo-2-pyrimidinyl)amino]carbonyl]amino]ethyl ester started to crystallize. The mixture was stirred for two and a half hour. 500 ml acetone was added and 3-methyl-2-propenoic acid-2-[[[(1,4-dihydro-6-methyl-4-oxo-2-pyrimidinyl)amino]carbonyl]amino]ethyl ester was isolated by filtration. 2-methyl-2-propenoic acid-2-[[[(1,4-dihydro-6-methyl-4-oxo-2-pyrimidinyl)amino]carbonyl]amino]ethyl ester was treated with 500 ml acetone, again isolated by filtration and dried. 68.6 g (82%) of 2-methyl-2-propenoic acid-2-[[[(1,4-dihydro-6-methyl-4-oxo-2-pyrimidinyl)amino]carbonyl]amino]ethyl ester was isolated (m.p.:208° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08192918B2uspto-grants-2012_06