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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658257Generated: October 27, 2026

Potassium Carbonate → tert-Butyl (3R,4S)-3-({cyclopropyl[3-[2-(dimethylamino)ethoxy]-5-(3-methoxypropyl)benzyl]amino}carbonyl)-4-{4-[2-(2,6-dichloro-4-methylphenoxy)-ethoxy]phenyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/658257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
Reactanttert-Butyl (3R,4S)-3-({cyclopropyl[3-hydroxy-5-(3-methoxypropyl)benzyl]-amino}carbonyl)-4-{4-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]phenyl}piperidine-1-carboxylateHCID 68492454—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Producttert-Butyl (3R,4S)-3-({cyclopropyl[3-[2-(dimethylamino)ethoxy]-5-(3-methoxypropyl)benzyl]amino}carbonyl)-4-{4-[2-(2,6-dichloro-4-methylphenoxy)-ethoxy]phenyl}piperidine-1-carboxylateHCID 86639855—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of tert-butyl (3R,4S)-3-({cyclopropyl[3-hydroxy-5-(3-methoxy-propyl)benzyl]amino}carbonyl)-4-{4-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]-phenyl}piperidine-1-carboxylate (1 eq.) from Example 1/Step 2 in DMF was added potassium carbonate (4.4 eq.) and 2-chloro-N,N-dimethylethanamine hydrochloride (2.5 eq.). The reaction was heated to 80° C. and stirred for 4 hr. After cooling to rt, the reaction was diluted with ether. The organic extract was washed with 5% aqueous potassium carbonate solution, brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by flash column chromatography (SiO2, 2%→5% [2 M NH3 in MeOH] in DCM) to afford the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076359B2
Source datasetuspto-grants-2011_12
ORD IDord-6b6d9c294f1e479a9b2ef2de14a68fd6
Source noteuspto-grants-2011_12