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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511831Generated: October 26, 2026

Triethylamine → rac-(2'R,3'S,4'S,5'R)-6-chloro-4'-(3-chloro-2-fluoro-phenyl)-2'-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-5'-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1511831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(3Z)-6-Chloro-3-[(3-chloro-2-fluorophenyl)methylidene]-1,3-dihydro-2H-indol-2-oneHCID 71464325—
ReactantHCID 178444818HCID 178444818—
SolventDichloromethaneHCID 6344—
Productrac-(2'R,3'S,4'S,5'R)-6-chloro-4'-(3-chloro-2-fluoro-phenyl)-2'-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-5'-carboxylic acid tert-butyl esterHCID 66625552—

Reaction Steps

To a solution of [3,3-dimethyl-but-(E)-ylideneamino]-acetic acid tert-butyl ester (2 g, 9.4 mmol) prepared in Example 1 and E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-1,3-dihydro-indol-2-one (2.3 g, 7.5 mmol) prepared in Example 2 in dichloromethane (30 mL) were added triethyl amine (2.8 mL, 20 mmol) and AgF (1.1 g, 8.7 mmol). The mixture was stirred at room temperature for 3 h. The mixture was concentrated, and the residue was partitioned between ethyl acetate and brine. The organic layer was separated, washed with water, dried over MgSO4, and concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:3, 1:2) to give as rac-(2′R,3′S,4′S,5′R)-6-chloro-4′-(3-chloro-2-fluoro-phenyl)-2′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-5′-carboxylic acid tert-butyl ester a white foam (1.9 g, 49%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217044B2
Source datasetuspto-grants-2012_07
ORD IDord-9645a335b5234ad2afe6b54bf72c6ba9
Source noteuspto-grants-2012_07