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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246956Generated: November 1, 2026

Dimethylcarbamoyl Chloride → HCID 86621622, compound

https://huagongshe.com/reaction/2246956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantPotassium hydrideHCID 82127—
ReactantHCID 68441031HCID 68441031—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86621622HCID 86621622—

Reaction Steps

To a solution of 100 mg of (R)-1-[(2R,4R,5R)-4-(4-methoxy-phenyl)-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-1-(toluene-4-sulfonyl)-piperidin-2-yl]-propan-2-ol (diastereomer 1) (from example 34b) in 10 ml tetrahydrofuran, are added 35 mg of potassium hydride and 0.14 ml of N,N-dimethylcarbamoyl chloride at room temperature. The reaction mixture is stirred for one additional hour, diluted with water and extracted with tert-butyl methyl ether. The combined organic phases are dried and concentrated under reduced pressure to afford the crude title compound. The residue is purified by flash chromatography (SiO2 60 F) to afford the title compound as a yellow oil. Rf=0.37 (EtOAc-heptane 2:1); Rt=5.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687495B2
Source datasetuspto-grants-2010_03
ORD IDord-04aea050b4a947ccb0aa4c645a9db6d4
Source noteuspto-grants-2010_03