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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183291Generated: October 25, 2026

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

https://huagongshe.com/reaction/2183291

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(2-Furylcarbonylamino)phenyl]-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamideHCID 22480223—
SolventTolueneHCID 1140—
Product3-[3-(2-Furylcarbonylamino)Phenyl]-1H-Indazole-5-CarboxamideHCID 2247983354%

Reaction Steps

3-[3-(2-Furylcarbonylamino)phenyl]-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carboxamide was suspended in 10 mL of toluene and HCl gas was bubbled through for 15 min. The reaction mixture was stirred at room temperature overnight. After neutralization with aqueous NaHCO3, the reaction mixture was evaporated to dryness and purified by preparatory HPLC. (0.111 g, 54% yield): 1H NMR (DMSO d6) δ 13.5 (br s, 1H), 10.3 (s, 1H), 8.64 (s, 1H), 8.4 (s, 1H), 8.11 (br s, 1H), 7.97 (s, 1H), 7.92 (t, 2H), 7.8 (d, 1H), 7.6 (d, 1H), 7.52 (t, 1H), 7.39 (d, 1H), 7.36 (s, 1H), 6.7 (t, 1H); ES-MS (m/z) 347 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-dc210e2c6c144be0bd6385975e019b07
Source noteuspto-grants-2005_05