m-Aminoacetanilide → N-(3-{[3-(acetylamino)phenyl]carbamoyl}phenyl)-3,6,8,9-tetrahydro-7H-pyrazolo[3,4-c][2,7]naphthyridine-7-carboxamide

Participants

Role	Name	HCID	Charge
Reactant	m-Aminoacetanilide	HCID 7604	—
Reactant	3-(3-(4-methoxybenzyl)-6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c][2,7]naphthyridine-7-carboxamido)benzoic acid	HCID 59490452	—
Product	N-(3-{[3-(acetylamino)phenyl]carbamoyl}phenyl)-3,6,8,9-tetrahydro-7H-pyrazolo[3,4-c][2,7]naphthyridine-7-carboxamide	HCID 59490601	—

Reaction Steps

The compound N-(3-{[3-(acetylamino)phenyl]carbamoyl}phenyl)-3,6,8,9-tetrahydro-7H-pyrazolo[3,4-c][2,7]naphthyridine-7-carboxamide was prepared using 3-(3-(4-methoxybenzyl)-6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c][2,7]naphthyridine-7-carboxamido)benzoic acid and N-(3-aminophenyl)acetamide as described in general procedure J. The compound was obtained as a solid. LCMS [M+H]: 470.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US08263610B2
Source dataset	uspto-grants-2012_09
ORD ID	ord-d4b9c08cb30f46dfb93d9a2bb2086b96
Source note	uspto-grants-2012_09