Реакция #58707

ord-6f8f55cface340e9901090f51f5175a9

Уравнение реакции

CCOC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1
mixture
CCOC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1
Ethyl 3-anilino-6-oxo-7-(3-thienyl)-6,7-dihydrothieno[2,3-b]pyridine-2-carboxylate
CCOCCO
2-ethoxyethanol
N
ammonia
NC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1
title compound
NC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1
3-Anilino-6-oxo-7-(3-thienyl)-6,7-dihydrothieno[2,3-b]pyridine-2-carboxamide

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe volatiles were removed in vacuo
  2. 2
    Другоеthe residue purified by column chromatography (silica, 50% to 100% EtOAc in hexane)

Методика

A mixture of Example 64 (129 mg), 2-ethoxyethanol and liquid ammonia was placed in a sealed pressure vessel and heated at 80° C. and 400 p.s.i. for 24 h. The volatiles were removed in vacuo and the residue purified by column chromatography (silica, 50% to 100% EtOAc in hexane) to give the title compound (20 mg). δH (CDCl3) 8.75 (1H, br s), 7.36-7.34 (2H, m), 7.16-7.11 (2H, m), 7.03 (1H, d, J 9.7 Hz), 6.99-6.88 (4H, m), 6.17 (1H, d, J 9.7 Hz), 5.47 (2H, br s). LCMS (ES+) RT 2.927 minutes, 368 (M+H)+

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07423047B2uspto-grants-2008_09