HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133005Generated: November 1, 2026
Tetrahydrofuran → HCID 178517114, compound
https://huagongshe.com/reaction/133005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | anthra(1,9-cd)pyrazol-6(2H)-one | HCID 8515 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 178517114 | HCID 178517114 | 25.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07390797B2 |
|---|
| Source dataset | uspto-grants-2008_06 |
|---|
| ORD ID | ord-a7299b688e6945bd80f75dc9229363ba |
|---|
| Source note | uspto-grants-2008_06 |
|---|