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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728063Generated: October 30, 2026

Trifluoroacetic acid → racemic (2'R,3R,4'S)-1'-[3-(4-acetyl-piperazin-1-yl)-propyl]-6-chloro-4'-(3-chlorophenyl)-2'-isopropenyl spiro[3H-indole-3,3' piperidine]-2,6'(1H)-dione

https://huagongshe.com/reaction/1728063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-AcetylpiperazineHCID 83795—
Reactant(2'R,3R,4'S)-6-chloro-4'-(3-chloro-phenyl)-1'-(3-chloro-propyl)-2'-isopropenyl-2,3-dihydro-2,6'-dioxospiro[indole-3,3'-piperidine] 1-methoxyethyl trimethylsilaneHCID 68958092—
ProductDiisopropylethylamineHCID 81531—
Productracemic (2'R,3R,4'S)-1'-[3-(4-acetyl-piperazin-1-yl)-propyl]-6-chloro-4'-(3-chlorophenyl)-2'-isopropenyl spiro[3H-indole-3,3' piperidine]-2,6'(1H)-dioneHCID 76568120166.8%

Reaction Steps

In a manner similar to the method described in example 60b, (2′R,3R,4′S)-6-chloro-4′-(3-chloro-phenyl)-1′-(3-chloro-propyl)-2′-isopropenyl-2,3-dihydro-2,6′-dioxospiro[indole-3,3′-piperidine]-1-methoxyethyl trimethylsilane prepared in example 123a (0.2 g, 0.20 mmol) was reacted with 1-piperazin-1-yl-ethanone (0.51 g, 4 mmol), trifluoroacetic acid (2 mL) and then N,N′-diisopropylethylamine (2 mL) to give racemic (2′R,3R,4′S)-1′-[3-(4-acetyl-piperazin-1-yl)-propyl]-6-chloro-4′-(3-chlorophenyl)-2′-isopropenylspiro[3H-indole-3,3′ piperidine]-2,6′(1H)-dione as a yellow solid (Yield: 95 mg, 50.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-8691cd2fbb744dbebf074dd8d0cf1592
Source noteuspto-grants-2009_02