Formamidine acetate → 5-Chloropyrimidine-4-carboxylic acid

HRID 614379노트

반응식

HRID 614379 반응식
C[O-].[Na+].[C:4]([OH:12])(=[O:11])/[C:5](=[C:7](\[CH:9]=O)/[Cl:8])/Cl.C(O)(=O)C.[CH:17]([NH2:19])=[NH:18]>CO>[C:4]([C:5]1[C:7]([Cl:8])=[CH:9][N:19]=[CH:17][N:18]=1)([OH:12])=[O:11]

참가 물질

5

실험 절차

Sodium methoxide (162 g) is added to a solution of mucochloric acid (169 g) and formamidine acetate (208 g) in methanol (3 liters) over the course of 20 minutes, and the reaction mixture is heated for 1 hour at 35°-40° C., and then for one and a half hours under reflux. The solvent is removed and water (500 cc) is added to the residue. The aqueous mixture is extracted with ethyl acetate (2 liters). The aqueous phase is brought to pH 1 by the addition of concentrated hydrochloric acid, and the aqueous phase is extracted with ethyl acetate (5 liters). The organic phase is dried over anhydrous magnesium sulphate, filtered and then concentrated to dryness. The residue is washed with diethyl ether (300 cc) and then with diisopropyl ether (600 cc). 4-Carboxy-5-chloropyrimidine (55.6 g), melting at 190° C., is obtained.

후처리

  1. temperaturethe reaction mixture is heated for 1 hour at 35°-40° C.
  2. temperaturefor one and a half hours under reflux
  3. customThe solvent is removed
  4. additionwater (500 cc) is added to the residue
  5. extractionThe aqueous mixture is extracted with ethyl acetate (2 liters)
  6. additionThe aqueous phase is brought to pH 1 by the addition of concentrated hydrochloric acid
  7. extractionthe aqueous phase is extracted with ethyl acetate (5 liters)
  8. dry with materialThe organic phase is dried over anhydrous magnesium sulphate
  9. filtrationfiltered
  10. concentrationconcentrated to dryness
  11. washThe residue is washed with diethyl ether (300 cc)

출처 및 근거

ORD 기록
ord-3a46c32cb00c48b088a319e662afffb7
출처 데이터셋
uspto-grants-1979_03
특허 번호
US04144339

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