Reacción #2196221

ord-2165f6df56cc4e908eff36551565e510

Ecuación de reacción

O=C(CCCCN1CCOCC1=O)Nc1c(C(=O)Nc2ccc(Cl)cn2)oc2ccc(C(=O)O)nc12
2-{[(5-Chloropyridin-2-yl)amino]carbonyl}-3-{[5-(3-oxomorpholin-4-yl)pentanoyl]amino}furo[3,2-b]pyridine-5-carboxylic acid
CNCCOC
N-(2-methoxyethyl)methylamine
→
COCCN(C)C(=O)c1ccc2oc(C(=O)Nc3ccc(Cl)cn3)c(NC(=O)CCCCN3CCOCC3=O)c2n1
title compound
Rendimiento 75.0%
COCCN(C)C(=O)c1ccc2oc(C(=O)Nc3ccc(Cl)cn3)c(NC(=O)CCCCN3CCOCC3=O)c2n1
N2-(5-Chloropyridin-2-yl)-N5-(methoxyethyl)-N5-methyl-3-{[5-(3-oxomorpholin-4-yl)pentanoyl]amino}furo[3,2-b]pyridine-2,5-dicarboxamide
Rendimiento 75.0%

Reactantes

O=C(CCCCN1CCOCC1=O)Nc1c(C(=O)Nc2ccc(Cl)cn2)oc2ccc(C(=O)O)nc12
2-{[(5-Chloropyridin-2-yl)amino]carbonyl}-3-{[5-(3-oxomorpholin-4-yl)pentanoyl]amino}furo[3,2-b]pyridine-5-carboxylic acid
CNCCOC
N-(2-methoxyethyl)methylamine

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

2-{[(5-Chloropyridin-2-yl)amino]carbonyl}-3-{[5-(3-oxomorpholin-4-yl)pentanoyl]amino}furo[3,2-b]pyridine-5-carboxylic acid (82 mg) obtained in Example 139 and N-(2-methoxyethyl)methylamine (28 mg) are treated in a similar manner to Example 85 to give the title compound (70 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07514449B2uspto-grants-2009_04