HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1273009Generated: October 30, 2026
HCID 69421897, compound → HCID 69420612, compound
https://huagongshe.com/reaction/1273009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69421897 | HCID 69421897 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 69420612 | HCID 69420612 | 13% |
Reaction Steps
3-[3-(2-Piperidylethoxy)phenyl]-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamide (0.61 g, 1.4 mmol) was suspended in 10 mL of 4 M HCl in dioxane and the suspension was stirred at room temperature for 18 h. The reaction was quenched with saturated aqueous solution of NaHCO3 and extracted with EtOAc. The organic layer was dried (Na2SO4) and filtered. The filtrate was concentrated and purification of the residue by preparative HPLC (20–80% acetonitrile in water) furnished 65 mg (13% yield) of the title compound. 1H NMR (DMSO-d6) δ 13.4 (br s, 1H), 8.6 (s, 1H), 8.2 (s, 1H), 7.94 (dd, 1H), 7.62 (m, 2H), 7.5 (m, 1H), 7.45 (t, 1H), 7.32 (br s, 1H), 7.05 (dd, 1H), 4.18 (t, 2H), 2.7 (m, 2H), 2.5 (m, 4H), 1.5 (m, 4H), 1.4 (m, 2H); ES-MS (m/z) 365 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208513B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-1c5c1fb277774f50a66336f50903a720 |
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| Source note | uspto-grants-2007_04 |
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