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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528993Generated: November 1, 2026

Benzyl acetone → [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-(1-methyl-3-phenyl-propyl)-amine

https://huagongshe.com/reaction/1528993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl acetoneHCID 17355—
Reactant5-(4-Bromophenyl)-3-methylisoxazol-4-amineHCID 58218537—
Product[5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-(1-methyl-3-phenyl-propyl)-amineHCID 66577220—

Reaction Steps

Prepared according to the procedure described in Example 24, Step 1, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and 4-phenyl-butan-2-one. After the reaction the crude material was purified via preparatory chiral HPLC (Chiralcel-AD column, 2% EtOH in hexanes, 25 minutes) to afford two separate enantiomers. The first enantiomer eluted from the column is the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090573B2
Source datasetuspto-grants-2015_07
ORD IDord-59dfdf9b73db4f3986113b6cc3096448
Source noteuspto-grants-2015_07