Реакция #58708

ord-cda9ed844bfe4417b80bbaeb2574e8fb

Уравнение реакции

CCOC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1C#N
mixture
CCOC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1C#N
Ethyl 3-[(2-cyanophenyl)amino]-6-oxo-7-(3-thienyl)-6,7-dihydrothieno[2,3-b]pyridine-2-carboxylate
CCOCCO
2-ethoxyethanol
N
ammonia
N#Cc1ccccc1Nc1c(C(N)=O)sc2c1ccc(=O)n2-c1ccsc1
title compound
N#Cc1ccccc1Nc1c(C(N)=O)sc2c1ccc(=O)n2-c1ccsc1
3-[(2-Cyanophenyl)amino]-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, EtOAc)

Методика

A mixture of Example 66 (100 mg), 2-ethoxyethanol and liquid ammonia was placed in a sealed pressure vessel and heated at 80° C. and 400 psi for 48 h. The volatiles were removed in vacuo and the residue purified by column chromatography (silica, EtOAc) to give the title compound (30 mg). δH (CDCl3) 7.59-7.46 (4H, m), 7.28-7.21 (3H, m), 7.20 (1H, t, J 2.0 Hz), 7.01 (1H, d, J 8.3 Hz), 6.49 (1H, d, J 9.7 Hz), 5.55 (2H, br s). LCMS (ES+) RT 2.845 minutes, 392.9 (M+H)+

Источник

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