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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550065Generated: October 30, 2026

3-amino-N-cyclopropyl-4-methylbenzamide → 5-(benzyloxy)-N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}pyridine-2-carboxamide

https://huagongshe.com/reaction/550065

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-amino-N-cyclopropyl-4-methylbenzamideHCID 11983854—
Reactant5-(Benzyloxy)pyridine-2-carboxylic acidHCID 18379352—
Product5-(benzyloxy)-N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}pyridine-2-carboxamideHCID 11406952—

Reaction Steps

The title compound was prepared from 5-(benzyloxy)pyridine-2-carboxylic acid and 3-amino-N-cyclopropyl-4-methylbenzamide according to the method described for Example 1; NMR Spectrum: (DMSOd6) 0.58 (m, 2H), 0.69 (m, 2H), 2.32 (s, 3H), 2.86 (m, 1H), 5.32 (s, 2H), 7.39 (m, 4H), 7.51 (m, 2H), 7.57 (m, 1H), 7.71 (m, 1H), 8.13 (m, 1H), 8.22 (m, 1H), 8.36 (m, 1H), 8.48 (s, 1H), 10.16 (s, 1H); Mass Spectrum: M+Na+424.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943776B2
Source datasetuspto-grants-2011_05
ORD IDord-979d1fee1a4b47919153ec3ffcabbdc0
Source noteuspto-grants-2011_05