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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376487Generated: October 30, 2026

2-Acetyl-5-bromothiophene → N-(7-(5-Acetyl-2-thienyl)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide

https://huagongshe.com/reaction/2376487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Acetyl-5-bromothiopheneHCID 79335—
Reactant(5-((3,3-Dimethylbutanoyl)amino)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-7-yl)boronic acidHCID 23114225—
SolventEthyl acetate hexaneHCID 21226206—
ProductN-(7-(5-Acetyl-2-thienyl)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamideHCID 2311393465%

Reaction Steps

Using (5-((3,3-dimethylbutanoyl)amino)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-7-yl)boronic acid obtained in Example 116 and 2-acetyl-5-bromothiophene, the title compound was synthesized in the same manner as in Example 107. Yield: 65%. Melting point: 157-158° C. (hexane-ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465815B2
Source datasetuspto-grants-2008_12
ORD IDord-3904f551fafc482bb9289aa2de270d85
Source noteuspto-grants-2008_12