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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408865Generated: October 31, 2026

Water → Methyl 5-(6-methylpyrazine-2-carboxamido)bicyclo[3.2.1]octane-1-carboxylate

https://huagongshe.com/reaction/1408865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-Methylpyrazine-2-carboxylic acidHCID 470897—
ReactantPyBOPHCID 2724699—
ReactantMethyl 5-aminobicyclo[3.2.1]octane-1-carboxylateHCID 68048077—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(6-methylpyrazine-2-carboxamido)bicyclo[3.2.1]octane-1-carboxylateHCID 6804807979%

Reaction Steps

To a solution of methyl 5-aminobicyclo[3.2.1]octane-1-carboxylate (0.98 g, 5.36 mmol) and 6-methylpyrazine-2-carboxylic acid (0.89 g, 6.45 mmol) in DCM (30 mL) and TEA (2 mL) was added PyBOP (3.35 g, 6.44 mmol). After stirring at room temperature overnight, water (30 mL) was added and the mixture was extracted with DCM (3×50 mL). The combined organic layer was washed with Sat. NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate: 1/1) to afford 1.28 g (79%) of methyl 5-(6-methylpyrazine-2-carboxamido)bicyclo[3.2.1]octane-1-carboxylate as an off-white solid. ESI-MS m/z: 304 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921370B2
Source datasetuspto-grants-2014_12
ORD IDord-047823d033a44f1699b14b153abb83cd
Source noteuspto-grants-2014_12