HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677051Generated: November 3, 2026
Hydrochloric Acid → 2,2-Difluoro-7,8,9,10-tetrahydro-6H-[1,3]dioxolo[4,5-g]pyrido[4,3-b]indole
https://huagongshe.com/reaction/1677051
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Piperidone hydrochloride | HCID 3084851 | — |
| Reactant | (2,2-Difluoro-benzo[1,3]dioxol-4-yl)hydrazine | HCID 55279040 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,2-Difluoro-7,8,9,10-tetrahydro-6H-[1,3]dioxolo[4,5-g]pyrido[4,3-b]indole | HCID 57541293 | 14.6% |
Reaction Steps
The (2,2-difluoro-benzo[1,3]dioxol-4-yl)-hydrazine (753 mg, 4.00 mmol) and 4-piperidone hydrochloride (543 mg, 4.00 mmol) in ethanol (10 mL) were heated to reflux for 45 min. The 4M HCl in dioxane (2 mL) was added and heating continued for 2 h. A sample was removed and after bubbling HCl gas briefly was heated in the microwave to 110° C. for 10 min. The rest of the material was processed in 5 batches and the combined black reactions filtered, washed with a little water and then precipitation with Et2O:Hexane 1:2 (c.f. 10 mL) before drying the resulting grey solid (147 mg, 13% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008279B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d2a9314bb3b844229d3a8059b3b86a67 |
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| Source note | uspto-grants-2011_08 |
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