تفاعل #82045

ord-23e01b0142a94f9da7c8d1326042622e

معادلة التفاعل

Nc1cc(Cl)cc(C(F)(F)F)c1N
2,3-diamino-5-chlorobenzotrifluoride
O.O.O=C(O)C(=O)O
oxalic acid dihydrate
O=c1[nH]c2cc(Cl)cc(C(F)(F)F)c2[nH]c1=O
title compound
المردود 50.5%
O=c1[nH]c2cc(Cl)cc(C(F)(F)F)c2[nH]c1=O
7-Chloro-5-trifluoromethyl-1,4-dihydro-2,3-quinoxalinedione
المردود 50.5%

الكواشف

لا شيء

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 by cold water (2×2 mL)
  4. 4
    ترشيحcollected by filtration
  5. 5
    أخرىdried at 60° C. for 2 h
  6. 6
    أخرىaffording 136 mg of crude title compound (53%) as a yellow powder
  7. 7
    ترشيحfiltered

الإجراء التجريبي

A mixture of 2,3-diamino-5-chlorobenzotrifluoride (180 mg, 0.86 mmol) and oxalic acid dihydrate (108 mg, 0.86 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 by cold water (2×2 mL), collected by filtration, and dried at 60° C. for 2 h, affording 136 mg of crude title compound (53%) as a yellow powder. The crude title compound was dissolved in 1N NaOH (6 mL) and filtered. The filtrate was acidified to pH =6, affording 115 mg of title compound. Recrystallization from DMSO/H2O gave 95 mg of pure title compound (37%) as yellow microcrystals. Mp: 302°-4° C. (dec. from 295° C.). IR (KBr, cm-1) 3401, 3255, 1754, 1694, 1528. 1H NMR (DMSO-d6): a 7.374 (d, 1H, J=1.8 Hz); 7.474 (d, 1H, J=1.8 Hz); 11.347 (s, 1H); 12.215 (s, 1H). HRMS: calcd for C9H4ClF3N2O2 (M+) m/z: 263.9912; found: 263.9909.

المصدر

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