تفاعل #79377

ord-ec32c99a8be345d8b67d0bb661f68654

معادلة التفاعل

O=c1[nH]c2cc(F)c(I)cc2c(=O)o1
4-fluoro-5-iodo-isatoic anhydride
CC(=O)O.N=CN
formamidine acetate
Oc1ncnc2cc(F)c(I)cc12
title compound
المردود 91.2%
Oc1ncnc2cc(F)c(I)cc12
4-Hydroxy-6-iodo-7-fluoroquinazoline
المردود 91.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfitted with a magnetic stir bar
  2. 2
    درجة الحرارةto cool
  3. 3
    تركيزby concentrating the reaction mixture to one third its original volume
  4. 4
    أخرىon the rotary evaporator
  5. 5
    workup.ADDITIONThe resulting mixture was poured onto 3 liters of ice water
  6. 6
    أخرىThe resulting precipitated solid
  7. 7
    ترشيحwas collected by suction filtration
  8. 8
    غسيلThe solid was washed with an additional one liter of distilled water
  9. 9
    أخرىThe resulting solid was dried under vacuum at 70° C.

الإجراء التجريبي

Dimethylformamide (0.5 liters), 4-fluoro-5-iodo-isatoic anhydride (45 grams, 147 mmoles), and formamidine acetate (45.92 grams, 441 mmoles), were combined in a one liter one-neck flask fitted with a magnetic stir bar. The mixture was placed under anhydrous nitrogen and heated at 110° C. for 6 hours. The mixture was allowed to cool, followed by concentrating the reaction mixture to one third its original volume on the rotary evaporator. The resulting mixture was poured onto 3 liters of ice water. The resulting precipitated solid was collected by suction filtration. The solid was washed with an additional one liter of distilled water. The resulting solid was dried under vacuum at 70° C. to yield 38.9 grams (91%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ: 12.43(s, 1H), 8.46(d, 1H), 8.12(s, 1H), 7.49(d, 1H). ESI-MS m/z 291(M+1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06713485B2uspto-grants-2004_03