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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055444Generated: November 3, 2026

Methanesulfonic acid pyridin-2-ylmethyl ester → 1'-[{6-Chloro-1-(pyridin-2-ylmethyl)-1H-indol-3-yl]carbonyl}-1,2-dihydrospiro[indole-3,4'-piperidine]

https://huagongshe.com/reaction/2055444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic acid pyridin-2-ylmethyl esterHCID 22417657—
Reactant1'-[(6-chloro-1H-indol-3-yl)carbonyl]-1,2-dihydrospiro[indole-3,4'-piperidine]HCID 59657691—
Product1'-[{6-Chloro-1-(pyridin-2-ylmethyl)-1H-indol-3-yl]carbonyl}-1,2-dihydrospiro[indole-3,4'-piperidine]HCID 59657607—

Reaction Steps

Following the general procedure III as described above, the alkylation of 1′-[(6-chloro-1H-indol-3-yl)carbonyl]-1,2-dihydrospiro[indole-3,4′-piperidine] (prepared according to example 8) with methanesulfonic acid pyridin-2-ylmethyl ester (described in WO 9955318) gave the title compound. ES-MS m/e (%): 457.2(M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-0fa107559e854889a90dd4e8a4564c4c
Source noteuspto-grants-2008_02