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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206560Generated: November 1, 2026

Cesium carbonate → HCID 89739691, compound

https://huagongshe.com/reaction/2206560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Fluoro-3-iodopyridineHCID 7009501—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
Reactant1269756-03-7HCID 89741572—
SolventDimethylacetamideHCID 31374—
Producttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
ProductHCID 89739691HCID 8973969134.4%

Reaction Conditions

Temperature125 °C

Reaction Steps

To a re-sealable vial containing 2-fluoro-3-iodopyridine (2.14 g, 9.60 mmol), (S)- or (R)-1-(tetrahydro-2H-pyran-4-yl)ethanaminium chloride (1.2175 g, 7.35 mmol) and cesium carbonate (7.54 g, 23.14 mmol) was added DMAc (10 mL). The vial was subsequently scaled and placed in a 125° C. bath. After stirring at 125° C. for 48 h, the reaction mixture was cooled to room temperature and partitioned between EtOAc with water. The aqueous layer was extracted with EtOAc (3×). The combined organic layers were washed with a minimal amount of water (2×), dried over Na2SO4, and concentrated to give a heterogeneous brown oil. The oil was diluted with EtOAc/Hexanes (1:3) and filtered. The solids were washed with EtOAc:Hexanes (1:3) and the filtrate was concentrated to give a brown oil. The resultant oil was purified on a Biotage system (40 g, gradient elution 2% EtOAc: 98% Hexanes to 10% EtOAc: 900 Hexanes, then isocratic 10% EtOAc: 90% Hexanes). The product (S)- or (R)-3-iodo-N-(1-(tetrahydro-2H-pyran-4-yl)ethyl)pyridin-2-amine (0.84 g, 2.53 mmol, 34.4% yield) was isolated as a clear colorless oil. LRMS (M+H+) m/z: calcd 333.0. found 333.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-21bac79d2a9b47eabea50ced803e5a09
Source noteuspto-grants-2016_06