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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364123Generated: October 26, 2026

Pyridine → 1,1-Dimethylethyl 2-[4-(methylsulfonyl)phenyl]-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6(2H)-carboxylate

https://huagongshe.com/reaction/1364123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
ReactantHCID 178451637HCID 178451637—
CatalystCupric acetateHCID 8895—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1,1-Dimethylethyl 2-[4-(methylsulfonyl)phenyl]-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6(2H)-carboxylateHCID 66930809—

Reaction Steps

A solution of 1,1-dimethylethyl 4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6(2H)-carboxylate (may be prepared as described in Description 9) (75 mg, 0.32 mmol), [4-(methylsulfonyl)phenyl]boronic acid (128 mg, 0.64 mmol), copper acetate (116 mg, 0.64 mmol), molecular sieves (4 Å, 0.2 g) and pyridine (52 μl, 0.64 mmol) in dichloromethane (2.5 ml) was stirred at room temperature open to atmosphere for 60 hours. The mixture was then diluted with methanol and filtered through a celite pad washing with methanol. The solvent was evaporated in vacuo. Residue was taken up into ethyl acetate and washed with water and 5% aq. sodium hydrogen carbonate, then dried over magnesium sulphate and evaporated in vacuo. The resulting residue was purified by MDAP to afford the title compound (D32). MS (ES+) m/e 392 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888347B2
Source datasetuspto-grants-2011_02
ORD IDord-262e5fd9920f4655ba69f171838244ef
Source noteuspto-grants-2011_02