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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095152Generated: October 30, 2026

Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester → HCID 178515582, compound

https://huagongshe.com/reaction/1095152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantZ-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl esterHCID 66640668—
ReactantHCID 178463709HCID 178463709—
SolventTolueneHCID 1140—
ProductHCID 178515582HCID 17851558242.7%

Reaction Steps

In a manner similar to the method described in example 1e, E/Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester prepared in example 1b (0.47 g, 1.2 mmol) was reacted 1-[2-[trans-4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyloxy]-5-chloro-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene (3 mmol) in toluene to give racemic(2′R, 3R, 4′S)-6-chloro-2′-[5-chloro-2-(cis-4-hydroxy-cyclohexyloxy)-phenyl]-4′-(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione as a pale yellow solid (Yield 0.3 g, 42%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-56a6626aa07d4c18a3f9371cf1d54b63
Source noteuspto-grants-2012_03