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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437931Generated: November 4, 2026

Picolinic acid → HCID 57941440, compound

https://huagongshe.com/reaction/1437931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
Reactant2-BromopyridineHCID 7973—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 57941341HCID 57941341—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
ProductHCID 57941440HCID 5794144025.9%

Reaction Steps

A mixture of (4S,7R)-1,7,8,8-tetramethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Intermediate 19; 412 mg, 2 mmol), 2-bromo-pyridine (175 μL, 1.8 mmol), copper(I) iodide (19 mg, 0.1 mmol), picolinic acid (49 mg, 0.4 mmol), and potassium bicarbonate (280 mg, 2.8 mmol) in N,N-dimethylformamide (10 mL) was irradiated in a microwave oven at 220° C. for 30 min. The reaction mixture was diluted with 0.1 M HCl (200 mL) and then extracted with ethyl acetate (200 mL). The organic layer was washed with 0.1 M HCl, 0.25 M NaOH, and brine, then dried (magnesium sulfate), filtered, evaporated and purified using an ISCO system, eluting with 5-60% ethyl acetate/dichloromethane to give (4S,7R)-2-(pyridin-2-yl)-1,7,8,8-tetramethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (132 mg, 23%) as a white solid. ES(+)-MS (M+H) 284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-e275c7950d2f4e419960eaa88cac21ab
Source noteuspto-grants-2009_11