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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504473Generated: October 25, 2026

6-Chloro-3-[5-chloro-2-(pyrimidin-2-yloxy)-benzylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester → 6-chloro-4'-[5-chloro-2-(pyrimidin-2-yloxy)-phenyl]-2'-(5-fluoro-2-methyl-phenyl)spiro[3H-indole-3,3'-piperidine]-2,6'(1H)-dione

https://huagongshe.com/reaction/504473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-3-[5-chloro-2-(pyrimidin-2-yloxy)-benzylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl esterHCID 67401774—
Reactant1-(5-Fluoro-2-methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadieneHCID 70178504—
SolventTolueneHCID 1140—
Product6-chloro-4'-[5-chloro-2-(pyrimidin-2-yloxy)-phenyl]-2'-(5-fluoro-2-methyl-phenyl)spiro[3H-indole-3,3'-piperidine]-2,6'(1H)-dioneHCID 749287903.5%

Reaction Steps

In a manner similar to the method described in example 1e, 6-chloro-3-[5-chloro-2-(pyrimidin-2-yloxy)-benzylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (1 g, 2 mmol) was reacted with 1-(5-fluoro-2-methylphenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene (10 mL, 20 mmol) in toluene to give title compound as a white solid (Yield: 40 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776875B2
Source datasetuspto-grants-2010_08
ORD IDord-dee6730eb58b46cd85adffaa90318e14
Source noteuspto-grants-2010_08