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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820144Generated: October 30, 2026

Azepane → HCID 11500844, compound

https://huagongshe.com/reaction/1820144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzepaneHCID 8119—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
ReactantN-(4-bromo-2,6-dimethyl-phenyl)-2-cyclopentyl-acetamideHCID 11507840—
ReactantSodium t-butoxideHCID 23676156—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
ProductHCID 11500844HCID 1150084450%

Reaction Conditions

Temperature110 °C

Reaction Steps

Bis(dibenzylideneacetone)palladium (2.8 mg) and (2′-dicyclohexylphosphanyl-biphenyl-2-yl)-dimethyl-amine (3.8 mg) were mixed in dry toluene (2.5 mL) under argon for 5 minutes. To this mixture were added sodium tert-butoxide (6 mg), azacycloheptane (7.5 mg) and N-(4-bromo-2,6-dimethyl-phenyl)-2-cyclopentyl-acetamide (1p, 15 mg) and the reaction was heated to 110° C. in a sealed 4 mL vial under argon for 48 hours. The reaction mixture was concentrated in vacuo, sodium hydroxide (2 M, 1.5 mL) was added and the product was extracted with isopropyl acetate (3×1.5 mL). The combined organic phases were dried over magnesium sulfate, concentrated in vacuo and purified by flash chromatography to furnish 7.9 mg (50% yield) of the title compound as an oil. LC-MS-TOF (m/z) 329 (MH+); tR=2.08, (UV, ELSD) 90%, 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601870B2
Source datasetuspto-grants-2009_10
ORD IDord-15509d4dd43e4553b70dd64df7aee6d7
Source noteuspto-grants-2009_10