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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095158Generated: October 31, 2026

Toluene → 4'-(3-chlorophenyl)spiro[3H-indole-3,3'-piperidine]-2,6'(1H)-dione

https://huagongshe.com/reaction/1095158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrifluoroacetic acidHCID 6422—
ReactantZ-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl esterHCID 66640668—
Reactant1-[5-Chloro-2-(tetrahydro-pyran-4-yloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadieneHCID 66641008—
SolventDichloromethaneHCID 6344—
Product4'-(3-chlorophenyl)spiro[3H-indole-3,3'-piperidine]-2,6'(1H)-dioneHCID 6862902364%

Reaction Steps

In a manner similar to the method described in example 32d, E/Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester prepared in example 5b (1.3 g, 3.3 mmol) was reacted with 1-[5-chloro-2-(tetrahydro-pyran-4-yloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene (8.3 mmol) in toluene, then treated with trifluoroacetic acid in dicloromethane to give racemic(2′R, 3R, 4′S)-6-chloro-2′-[5-chloro-2-(tetrahydro-pyran-4-yloxy)-phenyl]]-4′-(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione as a white solid (Yield 1.2 g, 64%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-39322ba8316a44489a74a45f31afc176
Source noteuspto-grants-2012_03