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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826369Generated: November 3, 2026

Diethyl Ether → HCID 9905321, compound

https://huagongshe.com/reaction/1826369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant3-Bromo-1-propanolHCID 12308—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl)methanesulfonamideHCID 22141143—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
ProductHCID 9905321HCID 990532129.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of the hydrochloride salt of N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl]methanesulfonamide (Preparation 53, 200 mg, 0.89 mmol) in N,N-dimethylformamide (8 ml) was added sodium hydrogen carbonate (3 g, 36 mmol) and 3-bromo-1-propanol (0.08 ml, 0.89 mmol), the reaction mixture was heated at 50° C. for 20 h. After cooling, diethyl ether (15 ml) and water (15 ml) were added and the reaction mixture was stirred vigorously for 5 min. The phases were separated and the aqueous layer was further extracted with diethyl ether (2×15 ml). The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo. The residual oil was purified by flash column chromatography using a Sep-Pak™ cartridge packed with silica gel (10 g) eluting with dichloromethane:ethanol:0.88 ammonia solution (200:8:1) to afford the title compound as an oil (42 mg, 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049444B2
Source datasetuspto-grants-2006_05
ORD IDord-5a3a2f36dbf6496cb8d2a5021a02e8a2
Source noteuspto-grants-2006_05