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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56536Generated: October 28, 2026

2-(4-Bromo-3,5-dimethoxyphenyl)furan → 1-(5-(4-Bromo-3,5-dimethoxyphenyl)furan-2-yl)-2-(4-(5-cyclopropyl-1,3,4-oxadiazol-2-yl)phenyl)-2-methoxyethanone

https://huagongshe.com/reaction/56536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Bromo-3,5-dimethoxyphenyl)furanHCID 58431988—
Reactant2-(4-(5-Cyclopropyl-1,3,4-oxadiazol-2-yl)phenyl)-N,2-dimethoxy-N-methylacetamideHCID 58432020—
Product1-(5-(4-Bromo-3,5-dimethoxyphenyl)furan-2-yl)-2-(4-(5-cyclopropyl-1,3,4-oxadiazol-2-yl)phenyl)-2-methoxyethanoneHCID 5843206031%

Reaction Steps

2-(4-(5-Cyclopropyl-1,3,4-oxadiazol-2-yl)phenyl)-N,2-dimethoxy-N-methylacetamide was reacted with 2-(4-bromo-3,5-dimethoxyphenyl)furan according to the procedure for the synthesis of Example 12. Purification by chromatography (EtOAc-hexanes) gave 1-(5-(4-bromo-3,5-dimethoxyphenyl)furan-2-yl)-2-(4-(5-cyclopropyl-1,3,4-oxadiazol-2-yl)phenyl)-2-methoxyethanone as a yellow foam (0.126 g, 31% yield). MS: m/z 539.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434707B2
Source datasetuspto-grants-2016_09
ORD IDord-d1b4e1d807024c7aa9db382690d91548
Source noteuspto-grants-2016_09