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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30306Generated: October 29, 2026

Aniline → (2-Oxo-1-(3-phenylamino-benzyl)-azepan-3-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/30306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant[1-(3-Iodo-benzyl)-2-oxo-azepan-3-yl]-carbamic acid tert-butyl esterHCID 23555228—
ReactantSodium t-butoxideHCID 23676156—
CatalystPalladium (II) acetateHCID 4144353—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventBinap, (A+-)-HCID 634876—
Product(2-Oxo-1-(3-phenylamino-benzyl)-azepan-3-yl]-carbamic acid tert-butyl esterHCID 68950358—

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 100 ml round bottomed flask Binap, (S)-(−)2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl, (0.210 g, 0.3375 mmol) dissolved in 15 mL toluene was stirred at 80° C. for 1 minute. To the flask cooled to room temperature under inert atmosphere Pd(OAC)2 (0.050 g, 0.225 mmol) was added and the solution was stirred at room temperature for 2 minutes. To the reaction mixture [1-(3-Iodo-benzyl)-2-oxo-azepan-3-yl]-carbamic acid tert-butyl ester (1.0 g, 2.25 mmol) dissolved in 15 mL toluene, aniline (1.047 g, 11.25 mmol) and Sodium tert-butoxide (0.259 g, 2.70 mmol) were added and the solution was stirred at 80° C. for 18 h. The reaction was cooled to room temperature, diluted with 200 mL of water, and extracted twice with 100 mL of ethyl acetate. The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated to an oil. The oil was purified on flash silica gel column using 10-30% ethyl acetate in hexanes as eluent to yield 0.562 g (61%). MS (ESI) M+H=432.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423033B2
Source datasetuspto-grants-2008_09
ORD IDord-cd1d4117fe8b431f866b08b35adbdc96
Source noteuspto-grants-2008_09