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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727970Generated: November 3, 2026

1-(3-Methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene → 6-Chloro-4'-(3-chlorophenyl)-2,3-dihydro-2'-(3-methylphenyl)-2,6'-dioxo spiro[indole-3,3'-piperidine]-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1727970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadieneHCID 70263764—
ReactantZ-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid ethyl esterHCID 86615084—
SolventTolueneHCID 1140—
Product6-Chloro-4'-(3-chlorophenyl)-2,3-dihydro-2'-(3-methylphenyl)-2,6'-dioxo spiro[indole-3,3'-piperidine]-1-carboxylic acid ethyl esterHCID 7656803586%

Reaction Steps

In a manner similar to the method described in example 4c, E/Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid ethyl ester (0.4 g, 1.10 mmol) prepared in example 4b was reacted with 1-(3-methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene prepared in example 10a, in toluene to give racemic (2′R,3R,4′S)-6-chloro-4′-(3-chlorophenyl)-2,3-dihydro-2′-(3-methylphenyl)-2,6′-dioxospiro[indole-3,3′-piperidine]-1-carboxylic acid ethyl ester as a yellow oil (Yield 0.5 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-5a7ea8f08e2a48ee9e59b3ad205fd3a3
Source noteuspto-grants-2009_02