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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696730Generated: October 31, 2026

Methylamine → 1-(6-Amino-4-bromo-pyridin-2-yl)-3-methyl-urea

https://huagongshe.com/reaction/1696730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTetrahydrofuranHCID 8028—
Reactant4-Bromo-2,6-diaminopyridineHCID 11435393—
SolventAcetonitrileHCID 6342—
Product1-(6-Amino-4-bromo-pyridin-2-yl)-3-methyl-ureaHCID 67273920—

Reaction Steps

To a solution of 0.188 g 2.6-diamino-4-bromopyridine in 2 ml acetonitrile was added 0.164 g 1,1-carbonyldi(1,2,4-triazole) and the mixture was stirred at room temperature. After a short period of a clear solution a suspension formed. The mixture was stirred at room temperature for 1 h. To the resulting suspension was added 0.5 ml of a methylamine solution in THF (ca 3 M) and the resulting solution was stirred at room temperature for 0.5 h. The mixture was partitioned between water and ethyl acetate. The phases were separated and the organic phase evaporated to dryness. The residue was taken up in methanol whereby crystallisation occurred. The crystals were collected by filtration and dried to constant weight to yield 0.196 g of the title compound as white crystals. MS (ISP) M+H+243.3; 245.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163778B2
Source datasetuspto-grants-2012_04
ORD IDord-3eda86f27f594dbaab1caf8e3c02fbe6
Source noteuspto-grants-2012_04