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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728209Generated: October 31, 2026

Ethyl Acetate → racemic (2'R,3R,4'S)-1'-(aminocarbonyl-methyl)-6-bromo-4'-(3-chlorophenyl)-2'-isopropenyl-2,3-dihydro-2,6'-dioxo spiro[indole-3,3'-piperidine] 1-methoxyethyl trimethylsilane

https://huagongshe.com/reaction/1728209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant2-BromoacetamideHCID 69632—
Reactantracemic (2'R,3R,4'S)-6-bromo-4'-(3-chlorophenyl)-2'-isopropenyl-2,3-dihydro-2,6'-dioxospiro[indole-3,3'-piperidine] 1-methoxyethyl trimethylsilaneHCID 77581434—
SolventDimethylformamideHCID 6228—
Productracemic (2'R,3R,4'S)-1'-(aminocarbonyl-methyl)-6-bromo-4'-(3-chlorophenyl)-2'-isopropenyl-2,3-dihydro-2,6'-dioxo spiro[indole-3,3'-piperidine] 1-methoxyethyl trimethylsilaneHCID 7758011255.6%

Reaction Steps

To a mixture of racemic (2′R,3R,4′S)-6-bromo-4′-(3-chlorophenyl)-2′-isopropenyl-2,3-dihydro-2,6′-dioxospiro[indole-3,3′-piperidine]-1-methoxyethyl trimethylsilane (100 mg, 0.17 mmol) and 2-bromo-acetamide (72 mg, 0.52 mmol) in DMF (1 mL) was added Cs2CO3 (332 mg, 1.01 mmol). The mixture was stirred at room temperature for overnight. Then additional 2-bromo-acetamide (72 mg, 0.52 mmol) and Cs2CO3 (332 mg, 1.01 mmol) were added to the reaction mixture. The resulting mixture was heated at 50° C. for 2 h, then poured into ethyl acetate (20 mL). The organic layer was washed with water 3 times, dried over Na2SO4, purified by column chromatography to give title compound 60 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-0d6a6391893243d0958191ebbc0f0998
Source noteuspto-grants-2009_02