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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656861Generated: October 26, 2026

Chloroform → 7-fluoro-1-(2-{4-[([1,3]oxathiolo[5,4-c]pyridin-6-ylmethyl)amino]-1-piperidinyl}ethyl)-2(1H)-quinolinone Dihydrochloride

https://huagongshe.com/reaction/656861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant[1,3]Oxathiolo[5,4-c]pyridine-6-carbaldehydeHCID 59254367—
Reactant1-[2-(4-Amino-1-piperidinyl)ethyl]-7-fluoro-2(1H)-quinolinoneHCID 66774406—
SolventMethanolHCID 887—
Product7-fluoro-1-(2-{4-[([1,3]oxathiolo[5,4-c]pyridin-6-ylmethyl)amino]-1-piperidinyl}ethyl)-2(1H)-quinolinone DihydrochlorideHCID 68992361—

Reaction Steps

A mixture of 1-[2-(4-amino-1-piperidinyl)ethyl]-7-fluoro-2(1H)-quinolinone (100 mg; 0.364 mmol) and [1,3]oxathiolo[5,4-c]pyridine-6-carbaldehyde (for a synthesis see WO2004058144, Example 61) (57 mg; 0.364 mmol) were dissolved in a 5:1 mixture of chloroform and methanol (5 ml: 1 ml) and stirred at rt under argon for 1 h. The mixture was then treated with NaBH(OAc)3 (231 mg; 1.092 mmol) and stirred for a further 1 h. The solvents were then removed and the crude residues purified by chromatography on silica gel using a 0-15% MeOH/DCM gradient to provide the title compound as free base (140 mg; 92%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-3b81060ee2224583b7e0e7b201b69d69
Source noteuspto-grants-2011_12