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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367346Generated: October 28, 2026

Diethylamine → HCID 53765795, compound

https://huagongshe.com/reaction/367346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromo-N,N-dimethylacetamideHCID 225544—
ReactantHCID 54072388HCID 54072388—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 53765795HCID 5376579578.4%

Reaction Steps

(-)-(1R)-1-[4-Benzyloxy-3-(2-benzyloxyethyl)phenyl]-2-((2S)-7-hydroxy-1,2,3,4-tetrahydronaphthalen-2-ylamino)ethanol (450 mg) was dissolved in 4 ml of methylene chloride, 860 μl of 5 N aqueous sodium hydroxide solution and 143 mg of 2-bromo-N,N-dimethylacetamide were added to the solution with stirring at room temperature in that order, and the mixture was subjected to 3 hours of reaction at room temperature. Then, 143 mg of 2-brorno-N,N-dimethylacetamide was additionally added to the reaction solution, and the mixture was subjected to 1 hour of reaction at room temperature. Then, 267 μl of diethylamine was added and the mixture was stirred for 30 minutes. Brine was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the resulting residue was purified by aminopropylated silica gel medium pressure liquid column chromatography (eluent: ethyl acetate) to give 410 mg of (-)-2-[(2S)-2-[[(2R)-2-[4-benzyloxy-3-(2-benzyloxyethyl)phenyl]-2-hydroxyethyl]amino]-1,2,3,4-tetrahydronaphthalen-7-yloxy)-N,N-dimethylacetamide in an oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133266
Source datasetuspto-grants-2000_10
ORD IDord-ea611ae2c8f4409aaf9b205bbf5b8da3
Source noteuspto-grants-2000_10