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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095103Generated: October 30, 2026

1-Pyrrolidineethanamine → HCID 74931454, compound

https://huagongshe.com/reaction/1095103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PyrrolidineethanamineHCID 1344—
Reactant4-MethylmorpholineHCID 7972—
ReactantHCID 74931420HCID 74931420—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 74931454HCID 7493145483%

Reaction Steps

In a manner similar to the method described in example 55b, racemic(2′R, 3R, 4′S)-2′-[5-bromo-2-(4-fluorocarbonyl-phenoxy)-phenyl]-6-chloro-4′-(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione (0.18 g, 0.28 mmol) was reacted with N-(2-aminoethyl)pyrrolidine (0.4 g, 3.5 mmol), N-methylmorpholine and 4-dimethylaminopyridine in tetrahydrofuran to give racemic(2′R, 3R, 4′S)-2′-{5-bromo-2-[4-(2-pyrrolidin-1-yl-ethylcarbamoyl)-phenoxy]-phenyl}-6-chloro-4′-(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione as a white solid (Yield 0.17 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-277463001f5c416e8b9e67ad294797d7
Source noteuspto-grants-2012_03