تفاعل #3229

ord-d22c33b8f7f941c2ae9d370668c316af

معادلة التفاعل

CCOC(=O)c1nc2ccc([N+](=O)[O-])cc2c(O)c1C(=O)OCC
diethyl 4-hydroxy-6-nitroquinoline-2,3-dicarboxylate
CC(=O)O
acetic acid
CCOC(=O)c1nc2ccc(N)cc2c(O)c1C(=O)OCC
title compound
المردود 75.3%
CCOC(=O)c1nc2ccc(N)cc2c(O)c1C(=O)OCC
Diethyl 6-amino-4-hydroxyquinoline-2,3-dicarboxylate
المردود 75.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas refluxed for 20 hr under a nitrogen atmosphere
  2. 2
    درجة الحرارةThe reaction mixture was cooled
  3. 3
    ترشيحfiltered
  4. 4
    تركيزthe filtrate was concentrated
  5. 5
    أخرىThe dark residue was chromatographed (eluant: methylene chloride/methanol; 98/2) over silical gel

الإجراء التجريبي

A stirred mixture of diethyl 4-hydroxy-6-nitroquinoline-2,3-dicarboxylate (4.4 g, 13 mM), powdered iron (6.6 g, 118 mM) and glacial acetic acid (18.5 g, 307 mM) in ethanol (80 mL) was refluxed for 20 hr under a nitrogen atmosphere. The reaction mixture was cooled and filtered and the filtrate was concentrated. The dark residue was chromatographed (eluant: methylene chloride/methanol; 98/2) over silical gel to provide (3.01 g, 75.3%) the title compound as light orange crystals, mp 219°-221° C.; MS(CI): 305 (M+H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733910uspto-grants-1998_03