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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133005Generated: November 1, 2026

Tetrahydrofuran → HCID 178517114, compound

https://huagongshe.com/reaction/133005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactantanthra(1,9-cd)pyrazol-6(2H)-oneHCID 8515—
ReactantEthyl AcetateHCID 8857—
ReactantSodium AzideHCID 33557—
SolventSulfuric AcidHCID 1118—
ProductHCID 178517114HCID 17851711425.3%

Reaction Steps

To a solution of 100 mg of 2,6-dihydrodibenzo[cd,g]indazol-6-one [CAS No. 129-56-6] in 0.6 ml concentrated sulfuric acid was added 78 mg of sodium azide [CAS No. 26628-22-8], followed by stirring at room temperature for 3 days. After adding ice, the reaction mixture was poured into a mixture solution of 100 ml of ethyl acetate and 10 ml of tetrahydrofuran and washed with saturated sodium hydrogen carbonate solution. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was dissolved in tetrahydrofuran, adsorbed by 3.5 g of silica gel and subjected to silica gel chromatography [Wako Gel C-200, 2 g]. The fractions of tetrahydrofuran-toluene [19:1 to 9:1] were concentrated, and the resulting powder was suspended in tetrahydrofuran-toluene. A powder was collected by filtration, and recrystallized from dimethylformamide-water, to give 27 mg of 6,7-dihydro-2H-benzo[6,7]azepino[5,4,3-cd]indazol-6-one as green needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390797B2
Source datasetuspto-grants-2008_06
ORD IDord-a7299b688e6945bd80f75dc9229363ba
Source noteuspto-grants-2008_06