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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814111Generated: October 25, 2026

(1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)(thiazol-2-yl)-methanol → 1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(2-thiazolylcarbonyl)indole

https://huagongshe.com/reaction/1814111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)(thiazol-2-yl)-methanolHCID 22504451—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(2-thiazolylcarbonyl)indoleHCID 2250442245.7%

Reaction Steps

To a solution of the compound obtained in Example 27 (5) (110 mg) in dichloromethane (20 ml), manganese dioxide (900 mg) was added at 15 to 30° C. and the mixture was stirred for 30 minutes. The reaction solution was then filtered through Celite and concentrated under reduced pressure. The resulting residue was subjected to silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) to obtain 50 mg of the desired products as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-209eb3bf37fd4423927b1bc3fc381db0
Source noteuspto-grants-2005_04