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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102736Generated: October 30, 2026

Pyrrolidine → HCID 68858354, compound

https://huagongshe.com/reaction/2102736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant6-Chloro-1,3-dihydroindol-2-oneHCID 736344—
ReactantHCID 86609724HCID 86609724—
SolventIsopropanolHCID 3776—
ProductHCID 68858354HCID 68858354—

Reaction Conditions

Temperature90 °C

Reaction Steps

A suspension of 6-chlorooxindole (0.71 g, 4.24 mmol) (Cresent Chem.), (3-oxo-butyl)-propyl-carbamic acid tert-butyl ester (1 g, 4.69 mmol) (Tyger Sci.), and pyrrolidine (0.1 g) (Aldrich) in 2-propanol (15 mL) was heated at 90° C. for 2 days. The mixture was allowed to cool to room temperature. The solvent was removed and the residue was purified by chromatography to give 4-(6-chloro-2-oxo-1,2-dihydro-indol-3-ylidene)-azepane-1-carboxylic acid tert-butyl ester as a brown solid. (Yield: 1.36 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-057b47a9ac0246c69b0bb452f386d147
Source noteuspto-grants-2009_08