Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646695Generated: October 30, 2026

3-Amino-6-bromo-N-methylpyrazine-2-carboxamide → HCID 68650263, compound

https://huagongshe.com/reaction/646695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-6-bromo-N-methylpyrazine-2-carboxamideHCID 15148121—
ReactantN-(Phenylmethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinecarboxamideHCID 68651461—
ProductHCID 68650263HCID 6865026338%

Reaction Steps

3-amino-N-methyl-6-(5-{[(phenylmethyl)amino]carbonyl}pyridin-3-yl)pyrazine-2-carboxamide was synthesized according to the procedure described above from N-(phenylmethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxamide and 3-amino-6-bromo-N-methyl-2-pyrazincarboxamide. Yield 38%. 1H NMR (400 MHz, d6-DMSO): 9.58 (d, 1H), 9.36 (t, 1H), 9.02 (m, 3H), 8.86 (t, 1H), 7.34 (m, 4H), 7.24 (m, 1H), 4.50 (d, 2H), 2.83 (d, 3H); MS (EI) for C19H18N6O2: 363 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-7221184bc7664a14ba04525b224d546c
Source noteuspto-grants-2010_04