تفاعل #82025

ord-4c5d952d5e704bfdac91a8ae748464b9

معادلة التفاعل

O=c1[nH]c2cc(Cl)cc(Cl)c2[nH]c1=O
5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione
NOS(=O)(=O)O
NH2OSO3H
Nn1c(=O)c(=O)[nH]c2c(Cl)cc(Cl)cc21
1-amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione
المردود 69.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was stirred at room temperature overnight
  2. 2
    ترشيحThe white precipitate was collected by filtration
  3. 3
    غسيلwashed
  4. 4
    workup.DISTILLATIONwith cold distilled water (0.5 mL)
  5. 5
    أخرىdried on rotavapor at 60° C. for 2 h

الإجراء التجريبي

The procedure of Wallace, R. G., Org. Prep. Proc. Int. 14: 269 (1982) was adapted. 5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione (52 mg, 0.225 mmole) was dissolved in 3N KOH (1 mL) at 60° C. for 0.5 h, and NH2OSO3H (30 mg, 0.265 mmole, Aldrich) in distilled water (0.5 mL) was dropwise added into above solution with stirring at 60° C. Some precipitate came out after 15 mins. The mixture was stirred at room temperature overnight. The white precipitate was collected by filtration, washed with cold distilled water (0.5 mL) and dried on rotavapor at 60° C. for 2 h affording crude 1-amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione (38 mg, 69%), which included a little of the isomer (4-amino-5,7-dichloro-2,3-quinoxalinedione) by 1H NMR (it is not known which isomer is present in a greater amount).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05620979uspto-grants-1997_04