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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668765Generated: October 30, 2026

3-Methoxyaniline → HCID 57825076, compound

https://huagongshe.com/reaction/1668765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyanilineHCID 10824—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 57825156HCID 57825156—
ReactantHCID 67346612HCID 67346612—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57825076HCID 57825076—

Reaction Conditions

Temperature100 °C

Reaction Steps

A microwave tube was charged with 4-(3-bromo-phenyl)-4-(4-isopropoxy-3-methyl-phenyl)-4,5-dihydro-oxazol-2-ylamine (Building Block L, 181 mg, 0.467 mmol, 1.0 eq), sodium tert-butoxide (89 mg, 0.933 mmol, 2.0 eq.), 2-di-t-butylphosphino-2′,4′,6′-tri-1-propyl-1,1′biphenyl (18 mg, 0.042 mmol, 0.042 eq.), tris(dibenzylideneacetone)dipalladium (10 mg, 0.012 mmol, 0.025 eq.) and 3-methoxyaniline (115 mg, 0.933 mmol, 2.0 eq.). After three vacuum-nitrogen cycles, toluene was introduced (1 mL), the tube was sealed and stirred at 100° C. for 16 hours. After cooling to room temperature, water (1 mL) and ethylacetate (1 mL) were added. The organic fraction of the reaction mixture was placed on an SCX column. This was then washed with dichloromethane/methanol. The desired product was obtained by eluting with 2 M ammonia in methanol. Fractions containing the compound were combined and the product purified further using preparative HPLC to yield 99 mg (31% yield) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989449B2
Source datasetuspto-grants-2011_08
ORD IDord-01356a7a0f0447b1ba0158bf3f7891f0
Source noteuspto-grants-2011_08