تفاعل #82051

ord-ff5771b2bc68468b973da63eda30837f

معادلة التفاعل

Nc1cc(Br)cc(C(F)(F)F)c1N
2,3-diamino-5-bromobenzotrifluoride
O.O.O=C(O)C(=O)O
oxalic acid dihydrate
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
title compound
المردود 71.4%
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
7-Bromo-5-trifluoromethyl-1,4-dihydro-2,3-quinoxalinedione
المردود 71.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas refluxed at 120°-5° C. for 3 h
  2. 2
    أخرىthe liquid layer was removed
  3. 3
    غسيلThe yellow solid was washed twice by cold water (2×2 mL)
  4. 4
    ترشيحcollected by filtration
  5. 5
    أخرىdried at 60° C. for 2 h
  6. 6
    أخرىaffording 150 mg of crude title compound (81.9%) as a red powder
  7. 7
    ترشيحfiltered

الإجراء التجريبي

A mixture of 2,3-diamino-5-bromobenzotrifluoride (150 mg, 0.612 mmol) and oxalic acid dihydrate (81 mg, 0.643 mmol, used as received) in 2N HCl (4 mL) was refluxed at 120°-5° C. for 3 h, then cooled to room temperature. The mixture was centrifuged and the liquid layer was removed. The yellow solid was washed twice by cold water (2×2 mL), collected by filtration, and dried at 60° C. for 2 h, affording 150 mg of crude title compound (81.9%) as a red powder. The crude compound was dissolved in 1N NaOH (6 mL) and filtered. The filtrate was acidified to pH=6, affording 135 mg of title compound. Recrystallization from DMSO/H2O gave 125 mg of pure title compound (68.3%) as red microcrystals. Mp: 307°-9° C. (dec. from 290° C.). IR (KBr, cm-1) 3412, 3250, 1756, 1706, 1606; 1H NMR (DMSO-d6): δ 7.514 (d, 1H, J=1.5 Hz); 7.556 (d, 1H, J=1.5 Hz); 11.342 (s, 1H); 12.220 (s, 1H). HRMS: calcd for C9H4BrF3N2O2 (M+) m/z: 307.9407; found: 307.9420.

المصدر

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