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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341462Generated: October 26, 2026

Isopropyl methanesulfonate → HCID 66803052, compound

https://huagongshe.com/reaction/341462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl methanesulfonateHCID 13551—
ReactantSodium hydrideHCID 24758—
ReactantHCID 66802888HCID 66802888—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66803052HCID 6680305239%

Reaction Steps

Sodium hydride (60% dispersion in mineral oil, 9 mg, 0.22 mmol) was added to a solution of 1-{3-[4-amino-6-(methyl-phenyl-amino)-[1,3,5]triazin-2-yl]-[1,2,4]oxadiazol-5-yl}-azetidin-3-ol (Intermediate 166, 50 mg, 0.147 mol) in anhydrous DMF (0.5 mL) at 0 C under nitrogen and the mixture was stirred for 10 min. A solution of propan-2-yl methanesulfonate (26.7 μL, 0.221 mmol) in anhydrous DMF (0.5 mL) was then added and the mixture was stirred at room temperature for 18 h. Further sodium hydride (60% dispersion in mineral oil, 9 mg, 0.22 mmol) and propan-2-yl methanesulfonate (26.7 μL, 0.221 mmol) were then added and the mixture was stirred at room temperature for 4 h. The mixture was diluted with EtOAc (10 mL) then washed with saturated aq. sodium carbonate (4×5 mL), brine (5 mL) and evaporated under vacuum. The crude residue was purified by flash chromatography (0-2% (7M ammonia in MeOH) in DCM) to afford the title compound as a light yellow glass (22 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-a35028d0569d4c7fa6cb7660c775dfc5
Source noteuspto-grants-2014_11