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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600542Generated: October 26, 2026

Potassium Carbonate → HCID 59761167, compound

https://huagongshe.com/reaction/600542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant(Azetidin-1-yl)(3-chloro-4-fluorophenyl)methanoneHCID 59346868—
Reactantmethyl 3-hydroxy-5-[(3S)-1-methyl-2-oxo-pyrrolidin-3-yl]oxy-benzoateHCID 59761136—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylacetamideHCID 31374—
ProductHCID 59761167HCID 5976116783%

Reaction Steps

A mixture of methyl 3-hydroxy-5-[(3S)-1-methyl-2-oxo-pyrrolidin-3-yl]oxy-benzoate (Intermediate 8) (265 mg, 1 mmol), azetidin-1-yl-(3-chloro-4-fluoro-phenyl)methanone (CAS no. 863454-79-9) (320 mg, 1.5 mmol) and potassium carbonate (276 mg, 2.0 mmol) in DMA (10 mL) was stirred at 120° C. for 16 hours. The solution was evaporated under reduced pressure. The residue was dissolved in ethyl acetate (50 mL), washed with water (3×20 mL), dried (MgSO4), filtered and the solvent removed under reduced pressure. The combined aqueous extracts were acidified with 2N hydrochloric acid, extracted with a mixture of ethyl acetate and DCM (1:1, 3×20 mL), washed with brine, dried (MgSO4), filtered and the solvent removed under reduced pressure. The residue from this was dissolved in THF (2 mL) and methanol (1 mL) and treated with 2M (trimethylsilyl)diazomethane (0.240 mL, 0.48 mmol) and stirred for 30 minutes. The solution was treated with acetic acid (1 drop), evaporated under reduced pressure. This residue was combined with that from the initial ethyl acetate extraction and purified by flash chromatography on silica eluting with 20-100% ethyl acetate in isohexane to afford the product (380 mg, 83%). m/z 459 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902200B2
Source datasetuspto-grants-2011_03
ORD IDord-0908eda74fd94552bc738c7b04ebb060
Source noteuspto-grants-2011_03