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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066883Generated: October 31, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 21196575, compound

https://huagongshe.com/reaction/1066883

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21196682HCID 21196682—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21196575HCID 2119657573.6%

Reaction Steps

A 1.00 g of 1-(2-azidoethyl)-4,5-dihydro-1H-thieno[2,3-g]indazole was dissolved in 30 ml of dioxane, 2.80 g of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone was added at room temperature, and the mixture was heated under reflux for 8 hours. The reaction mixture was cooled, poured into sodium bicarbonate aqueous solution and then extracted with chloroform. The organic layers were combined and dried with anhydrous magnesium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under a reduced pressure, and the resulting residue was purified by a silica gel column chromatography to give 0.73 g of 1-(2-azidoethyl)-1H-thieno[2,3-g]indazole as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245796B1
Source datasetuspto-grants-2001_06
ORD IDord-64bbe581bc904174b77acd4374c3f32a
Source noteuspto-grants-2001_06