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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243038Generated: November 1, 2026

Methylamine → 6'-{[(ethylamino)carbonyl]amino}-N-methyl-4'-(4-phenyl-1,3-thiazol-2-yl)-3,3'-bipyridine-5-carboxamide

https://huagongshe.com/reaction/2243038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant6'-{[(Ethylamino)carbonyl]amino}-4'-(4-phenyl-1,3-thiazol-2-yl)-3,3'-bipyridine-5-carboxylic acidHCID 59208341—
SolventDimethylformamideHCID 6228—
Product6'-{[(ethylamino)carbonyl]amino}-N-methyl-4'-(4-phenyl-1,3-thiazol-2-yl)-3,3'-bipyridine-5-carboxamideHCID 5920846348%

Reaction Steps

2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (73.7 mg, 0.19 mmol), DIEA (78.6 mg, 0.45 mmol) and methylamine (2M soln in THF, 0.15 mL, 0.30 mmol) were added to a solution of 6′-{[(ethylamino)carbonyl]amino}-4′-(4-phenyl-1,3-thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Example 132, 66.4 mg, 0.15 mmol) in DMF (1.5 mL). The resulting light yellow solution was stirred at room temperature for three hours. The reaction mixture was partitioned between water and ethyl acetate and layers separated. The organic layer was washed with saturated NaHCO3, water, brine, then dried over magnesium sulfate. The solvent was removed and the resulting residue was washed with acetonitrile and filtered to yield 33 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674801B2
Source datasetuspto-grants-2010_03
ORD IDord-4362ef5210c24d3b85c0d51b94ca5be1
Source noteuspto-grants-2010_03