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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523048Generated: October 30, 2026

5-chloro-1-(2-phenylethyl)-1H-indole-2,3-dione → 5-Chloro-3-hydroxy-3-((3-methoxypyridin-2-yl)methyl)-1-phenethylindolin-2-one

https://huagongshe.com/reaction/1523048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-chloro-1-(2-phenylethyl)-1H-indole-2,3-dioneHCID 2930041—
Reactant3-Methoxy-2-methylpyridineHCID 3015270—
Reactant3-((3-Bromopyridin-2-yl)methyl)-3-hydroxy-1-isopentyl-5-methylindolin-2-oneHCID 90418661—
Product5-Chloro-3-hydroxy-3-((3-methoxypyridin-2-yl)methyl)-1-phenethylindolin-2-oneHCID 86300398—

Reaction Steps

This compound was prepared in an analogous manner to 3-((3-bromopyridin-2-yl)methyl)-3-hydroxy-1-isopentyl-5-methylindolin-2-one using 5-chloro-1-phenethylindoline-2,3-dione and 3-methoxy-2-methylpyridine. 1H-NMR δ 8.21 (dd, 1H), 7.33-7.17 (m, 8H), 6.95 (d, 1H), 6.62 (d, 1H), 5.5 (bs, OH), 3.98 (m, 1H), 3.86 (m, 1H), 3.78 (s, 3H), 3.37 (d, 1H), 3.09 (d, 1H), 2.96 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079853B2
Source datasetuspto-grants-2015_07
ORD IDord-9c9983739c894e7caaf4cccdf1b342ec
Source noteuspto-grants-2015_07