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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095708Generated: October 30, 2026

Hydrochloric Acid → (trans)-4-(2-(7-(2-Methoxvethoxv)imidazo[1,2-a]pyridin-3-yl)quinolin-8-yloxy)pyrrolidin-3-ol

https://huagongshe.com/reaction/1095708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant(trans)-Naphthalen-2-ylmethyl 3-hydroxy-4-(2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinolin-8-yloxy)pyrrolidine-1-carboxylateHCID 131729511—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product(trans)-4-(2-(7-(2-Methoxvethoxv)imidazo[1,2-a]pyridin-3-yl)quinolin-8-yloxy)pyrrolidin-3-olHCID 2509843320.2%

Reaction Steps

A 25 mL flask was charged with (trans)-naphthalen-2-ylmethyl 3-hydroxy-4-(2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinolin-8-yloxy)pyrrolidine-1-carboxylate (0.100 g, 0.165 mmol), EtOH (1.6 mL), THF (1.6 mL), 2 N HCl (0.2 mL) and 10% Degussa type Pd/C (0.018 g, 0.017 mmol), and the reaction was placed under a balloon of H2 and stirred for 2 hours. The reaction was filtered (GF/F paper), the filter paper was washed with 2 N HCl and THF, the aqueous phase was washed with DCM, neutralized with saturated NaHCO3, and then extracted with DCM. The organic layer was dried and condensed to afford 14 mg of the desired product. MS APCI (+) m/z 421.2 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138181B2
Source datasetuspto-grants-2012_03
ORD IDord-7caf852f20864c8c885edf583a0ba40a
Source noteuspto-grants-2012_03