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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267502Generated: October 31, 2026

3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-[3-(hydroxymethyl)phenyl]-1H-indole-7-carboxamide → 3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-(3-formylphenyl)-1H-indole-7-carboxamide

https://huagongshe.com/reaction/2267502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-[3-(hydroxymethyl)phenyl]-1H-indole-7-carboxamideHCID 11605713—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-(3-formylphenyl)-1H-indole-7-carboxamideHCID 5900335565%

Reaction Steps

To a solution of 3-(1-{[3-(dimethylamino)propyl]sulfonyl}-4-piperidinyl)-5-[3-(hydroxymethyl)phenyl]-1H-indole-7-carboxamide (230 mg, 0.47 mmol) in THF (60 mL) was added MnO2 (1.3 g, 14.05 mmol). The reaction mixture was stirred at room temperature overnight and filtered through a pad of celite after that. The filtrate was collected and concentrated at reduced pressure to give the crude product (150 mg, 65%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858796B2
Source datasetuspto-grants-2010_12
ORD IDord-cc62cc7f843041a68530c3cb37189044
Source noteuspto-grants-2010_12