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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055521Generated: October 27, 2026

1-Piperidinecarbonyl chloride → 1'-{[6-Chloro-1-(piperidin-1-ylcarbonyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4'-piperidine]

https://huagongshe.com/reaction/2055521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Piperidinecarbonyl chlorideHCID 242085—
Reactant(6-chloro-1H-indol-3-yl)-spiro[1H-2-benzofuran-3,4'-piperidine]-1'-ylmethanoneHCID 15951937—
Product1'-{[6-Chloro-1-(piperidin-1-ylcarbonyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4'-piperidine]HCID 59657655—

Reaction Steps

Following the general procedure V as described hereinabove, the alkylation of 1′-[(6-chloro-1H-indol-3-yl)carbonyl]-3H-spiro[2-benzofuran-1,4′-piperidine] (the preparation of which have been described in example 69) with commercially available piperidine-1-carbonyl chloride as electrophile, the title compound was obtained as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-84dc6a10d3fe4647a2877c1d4a56b3a3
Source noteuspto-grants-2008_02