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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255164Generated: October 26, 2026

Sodium hydride → tert-Butyl {1-[2-(7-methoxy-4-oxoquinolin-1(4H)-yl)ethyl)piperidin-4-yl}carbamate

https://huagongshe.com/reaction/255164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAcetonitrile--water (1/1)HCID 18373917—
Reactant2-(4-((Tert-butoxycarbonyl)amino)piperidin-1-yl)ethyl methanesulfonateHCID 56834478—
ReactantHCID 178487715HCID 178487715—
SolventDimethylformamideHCID 6228—
Producttert-Butyl {1-[2-(7-methoxy-4-oxoquinolin-1(4H)-yl)ethyl)piperidin-4-yl}carbamateHCID 8664260133%

Reaction Steps

A solution of 7-methoxyquinolin-4-ol (Intermediate 10, 500 mg, 2.85 mmol) in dry DMF (10 mL) was treated at 0° C. with a cooling bath under stirring with sodium hydride (114 mg, 60% in oil, 2.85 mmol). The cooling bath was removed and the mixture was stirred for 30 minutes at room temperature. A solution of 2-{4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}ethyl methanesulfonate in DMF (Intermediate 6, 0.58 mmol/mL, 5 mL, 2.9 mmol) was added and the resulting solution was stirred over night at room temperature. DMF was removed under reduced pressure, the residue was taken up in ethyl acetate (100 mL) and saturated aqueous sodium hydrogen carbonate solution (30 mL) and the aqueous phase was back extracted three times with ethyl acetate (3×70 mL). The combined organic phases were dried over sodium sulfate. Some starting 7-methoxyquinolin-4-ol was precipitated from dichloromethane (30 mL) with hexanes (20 mL) and removed by filtration. The filtrate was concentrated to dryness under reduced pressure. Chromatography of the residue on silica gel with acetonitrile/water (15:1 to 10:1) gave 373 mg (33% yield) of the product as a colorless solid, mp 207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875715B2
Source datasetuspto-grants-2011_01
ORD IDord-76cb0eb1a6f84a57b8564bf7fd4cc62f
Source noteuspto-grants-2011_01