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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437967Generated: November 2, 2026

Pyridine → HCID 57941372, compound

https://huagongshe.com/reaction/1437967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 57250492HCID 57250492—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57941372HCID 5794137244.7%

Reaction Steps

A mixture of (4S,7R)-1-phenyl-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Intermediate 8; 1.00 g, 3.7 mmol), phenyl-boronic acid (0.94 g, 7.5 mmol), and copper(II) acetate (1.03 g, 5.6 mmol) in dichloromethane (10 mL) and pyridine (0.6 mL, 7.5 mmol) was stirred at room temperature for 2 days and then heated at reflux for 2 h. The reaction mixture was diluted with water and dichloromethane. The aqueous layer was extracted twice with dichloromethane, and the combined organic layers were washed with water, 10% copper(II) sulfate solution, water, and brine. The solution was then dried (magnesium sulfate), filtered, evaporated and purified using an Analogix Intelliflash 280 system (Analogix, Inc., Burlington, Wis.) with an Analytical Sales Aspire 90 g column, eluting with 10-50% ethyl acetate/hexanes to give (4S,7R)-7,8,8-trimethyl-1,2-diphenyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (0.57 g, 44%) as a light brown solid. ES(+)-MS (M+H) 345.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-7323e83a756f43139df47fec919181f1
Source noteuspto-grants-2009_11