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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523099Generated: October 30, 2026

3-((1H-indol-3-yl)methyl)-5-chloro-2-oxo-1-propylindolin-3-yl benzoate → 3-((1-benzoyl-1H-indol-3-yl)methyl)-3-hydroxy-5-methyl-1-propylindolin-2-one

https://huagongshe.com/reaction/1523099

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-((1H-indol-3-yl)methyl)-5-chloro-2-oxo-1-propylindolin-3-yl benzoateHCID 86301438—
ReactantHCID 90411032HCID 90411032—
Reactant5-Methyl-2-oxo-1-propylindolin-3-yl benzoateHCID 90417475—
Product3-((1-benzoyl-1H-indol-3-yl)methyl)-3-hydroxy-5-methyl-1-propylindolin-2-oneHCID 86301277—

Reaction Steps

This compound was made in a method analogous to 3-((1H-indol-3-yl)methyl)-5-chloro-2-oxo-1-propylindolin-3-yl benzoate using 5-methyl-2-oxo-1-propylindolin-3-yl benzoate and (1-benzoyl-1H-indol-3-yl)methyl benzoate. 1H-NMR δ 8.33 (d, 1H), 7.53 (m, 2H), 7.45-7.39 (m, 4H), 7.31 (dd, 1H), 7.29 (m, 1H), 7.17 (s, 1H), 7.08 (d, 1H), 6.59 (m, 2H), 3.53 (m, 1H), 3.40 (d, 1H), 3.29 (d, 1H), 3.20 (m, 1H), 2.77 (s, OH), 2.30 (s, 3H), 1.15 (m, 2H), 0.56 (t, 3H). Calculated mass for C28H26N2O3, 438.19. Observed 461.2 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079853B2
Source datasetuspto-grants-2015_07
ORD IDord-11e11d3323404a628aa6c6e21ffb2c25
Source noteuspto-grants-2015_07