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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507510Generated: November 1, 2026

2-Fluoropyridine → HCID 136504481, compound

https://huagongshe.com/reaction/1507510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 136504489HCID 136504489—
SolventDimethylformamideHCID 6228—
ProductHCID 136504481HCID 13650448141.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 25-mL round-bottom flask, was placed a solution of tert-butyl (3R)-3-[[5-(1,3-benzothiazol-2-yl)-6-oxo-2-(piperidin-4-yl)-1,6-dihydropyrimidin-4-yl]amino]piperidine-1-carboxylate (150 mg, 0.29 mmol, 1.00 equiv) in N,N-dimethylformamide (5 mL) and 2-fluoropyridine (114 mg, 1.17 mmol, 4.00 equiv). This was followed by the addition of potassium carbonate (81 mg, 0.59 mmol, 2.00 equiv). The resulting solution was stirred for 24 h at 100° C. The solids were filtered out. The resulting mixture was concentrated under reduced pressure. The residue was purified through a silica gel column with dichloromethane/methanol (50:1-20:1) to afford 70 mg of tert-butyl (3R)-3-[[5-(1,3-benzothiazol-2-yl)-6-oxo-2-[1-(pyridin-2-yl)piperidin-4-yl]-1,6-dihydropyrimidin-4-yl]amino]piperidine-1-carboxylate as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221809B2
Source datasetuspto-grants-2015_12
ORD IDord-3d10145ac3ee40a9b8b42cd2b5102243
Source noteuspto-grants-2015_12