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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408872Generated: October 31, 2026

2-Aminopyridine → 6-methyl-N-{5-[(pyridin-2-ylamino)carbonyl]bicyclo[3.2.1]oct-1-yl}pyrazine-2-carboxamide

https://huagongshe.com/reaction/1408872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
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—
Reactant5-(6-Methylpyrazine-2-carboxamido)bicyclo[3.2.1]octane-1-carboxylic acidHCID 67981030—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-methyl-N-{5-[(pyridin-2-ylamino)carbonyl]bicyclo[3.2.1]oct-1-yl}pyrazine-2-carboxamideHCID 7049741427.4%

Reaction Steps

To a solution of 5-(6-methylpyrazine-2-carboxamido)bicyclo[3.2.1]octane-1-carboxylic acid (intermediate 26, 100 mg, 0.35 mmol) and pyridin-2-amine (39 mg, 0.41 mmol) in DMF (5 mL) was added HATU (158 mg, 0.41 mmol) and DIPEA (0.5 mL). After stirring at room temperature for one hour, water (20 mL) was added, and the solution was extracted with ethyl acetate (3×20 mL). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The resulting residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate: 2/1) to yield 35 mg (27%) of 6-methyl-N-{5-[(pyridin-2-ylamino)carbonyl]bicyclo[3.2.1]oct-1-yl}pyrazine-2-carboxamide as a white solid. Analytical data were listed in Table 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921370B2
Source datasetuspto-grants-2014_12
ORD IDord-e15e445691db471998d913aa34acf284
Source noteuspto-grants-2014_12