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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183289Generated: October 26, 2026

1-Perhydro-2H-pyran-2-yl-3-[3-(3-piperidylpropanoylamino)phenyl]-1H-indazole-5-carboxamide → 3-[3-(3-Piperidylpropanoylamino)Phenyl]-1H-Indazole-5-Carboxamide

https://huagongshe.com/reaction/2183289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Perhydro-2H-pyran-2-yl-3-[3-(3-piperidylpropanoylamino)phenyl]-1H-indazole-5-carboxamideHCID 69425734—
SolventTolueneHCID 1140—
Product3-[3-(3-Piperidylpropanoylamino)Phenyl]-1H-Indazole-5-CarboxamideHCID 694208917%

Reaction Steps

1-Perhydro-2H-pyran-2-yl-3-[3-(3-piperidylpropanoylamino)phenyl]-1H-indazole-5-carboxamide was suspended in 20 mL of toluene and HCl gas was bubbled through for 15 min. The reaction mixture became gummy and was stirred at room temperature overnight. The supernatant solution was decanted and the residue was purified by preparatory HPLC. (0.017 g, 7% yield over 2 steps): 1H NMR (DMSO d6) δ 13.48 (s, 1H), 10.38 (s, 1H), 8.62 (s, 1H), 8.1 (s, 1H), 7.94 (dd, 1H), 7.94 (dd, 1H), 7.73 (d, 1H), 7.62 (d, 1H), 7.48 (t, 1H), 7.36 (br s, 1H), 2.65 (m, 2H), 2.5 (m, 2H), 2.4 (br s, 4H), 1.52 (m, 4H), 1.40 (m, 2H); ES-MS (m/z) 392 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-643f73dca919413b978e6045f17ba60f
Source noteuspto-grants-2005_05