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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339881Generated: October 25, 2026

(S)-1-Phenyl-3-propanolamine → HCID 178431680, compound

https://huagongshe.com/reaction/339881

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1-Phenyl-3-propanolamineHCID 2734520—
Reactant5-(3-Bromophenyl)-2-ethoxy-5-fluoro-6,6-dimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxideHCID 68359207—
SolventDichloromethaneHCID 6344—
ProductHCID 178431680HCID 17843168024.4%

Reaction Steps

In a round-bottom flask, 42 mg of 5-(3-bromophenyl)-2-ethoxy-5-fluoro-6,6-dimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide was dissolved under inert gas in 0.2 ml of dichloromethane and admixed with 20 mg of (S)-3-amino-3-phenylpropan-1-ol. After stirring at room temperature for 18 hours, the conversion was checked by LCMS. Since only traces of the product had formed, the reaction mixture was stirred at 100° C. for a further 4.5 hours. After the removal of the solvent under reduced pressure, the crude product was purified in a purification laboratory by means of preparative HPLC. The product-containing fractions were combined, the acetonitrile was removed under reduced pressure, and the aqueous residue was basified with saturated aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The organic phase was dried over MgSO4 and concentrated by rotary evaporation, and the residue was taken up again in a mixture of acetonitrile and water and lyophilized. This gave the product (13.1 mg) with a molecular weight of 485.4 g/mol (C20H22BrFN2O4S); MS (ESI): m/e=485 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895547B2
Source datasetuspto-grants-2014_11
ORD IDord-aeeab59a5351419c86fe8f6bc64b2a5b
Source noteuspto-grants-2014_11