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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353845Generated: October 25, 2026

3-[3-(2-methoxyacetylamino)phenyl]-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamide → 3-[3-(2-Methoxyacetylamino)Phenyl]-1H-Indazole-5-Carboxamide

https://huagongshe.com/reaction/1353845

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(2-methoxyacetylamino)phenyl]-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamideHCID 22480109—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
Product3-[3-(2-Methoxyacetylamino)Phenyl]-1H-Indazole-5-CarboxamideHCID 2247989240.5%

Reaction Steps

Through a suspension of 3-[3-(2-methoxyacetylamino)phenyl]-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamide in toluene (10 mL), HCl gas was bubbled for 20 min. After 6 hours at room temperature, the reaction was complete. The pH of the reaction mixture was neutralized using a saturated aqueous NaHCO3 solution before the solvent was removed under reduced pressure. The title compound was isolated as a white solid after purification by preparative HPLC (30–100% acetonitrile/water) (0.078 g, 40.5% yield): 1H NMR (CD3OD) δ 8.63 (dd, 1H), 8.19 (t, 1H), 7.94 (dd, 1H), 7.74 (td, 2H), 7.60 (dd, 1H), 7.49 (t, 1H), 4.06 (s, 2H), 3.49 (s, 3H); ES-MS (m/z) 325 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220771B2
Source datasetuspto-grants-2007_05
ORD IDord-91a35da176de4cf2b5db20623bcbfb33
Source noteuspto-grants-2007_05