تفاعل #1539

ord-28a790364d3a4b39a6924f5c3d8fb5d8

معادلة التفاعل

Cl.N=C(N)c1ccccc1.O
benzamidine hydrochloride hydrate
C[O-].[Na+]
sodium methoxide
CCOC(=O)C(CC)C(=O)OCC
diethyl ethylmalonate
CCc1c(O)nc(-c2ccccc2)[nH]c1=O
5-ethyl-6-hydroxy-2-phenyl-4(3H)-pyrimidinone
المردود 51.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةat reflux for 25 h
  3. 3
    أخرىto remove the bulk of the methanol
  4. 4
    workup.ADDITIONThe residue was diluted with 300 mL of water
  5. 5
    ترشيحThe solid precipitate was collected by filtration
  6. 6
    أخرىdried under vacuum at 50° C.

الإجراء التجريبي

A mixture of 45.19 g (0.29 mol) of benzamidine hydrochloride hydrate, 127.42 g (0.59 mol) of 25% sodium methoxide in methanol, 55 mL (0.29 mol) of diethyl ethylmalonate and 175 mL of methanol was heated at reflux for 25 h. The mixture was rotovapped to remove the bulk of the methanol. The residue was diluted with 300 mL of water and the pH was adjusted to 7 with concentrated hydrochloric acid. The solid precipitate was collected by filtration and dried under vacuum at 50° C. to afford 31.89 g (51%) of crude 5-ethyl-6-hydroxy-2-phenyl-4(3H)-pyrimidinone as a pale yellow solid. 1H-NMR (d6-DMSO) δ 1.05(3H,t), 2.39(2H,q), 7.5(3H,m), 8.1(2H,m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726124uspto-grants-1998_03