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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946983Generated: October 31, 2026

4-Nitro-1H-indole → HCID 59743448, compound

https://huagongshe.com/reaction/1946983

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-1H-indoleHCID 145766—
ReactantAcetone cardiceHCID 18522661—
ReactantAcetonitrile tetrahydrofuranHCID 22177404—
ReactantHCID 178503302HCID 178503302—
ProductHCID 59743448HCID 59743448—

Reaction Steps

A solution of sodium(bistrimethylsilyl)amide (1 M in THF, 26.42 mL) was slowly added to a cooled (acetone/dry-ice bath) solution of 4-nitroindole (4.2 g, 25.9 mmol) in a mixture of acetonitrile/THF (2/1, 75 mL) and the resulting mixture was stirred for 1 hour. 4-Chloro-4-methylthiopyrimidine (4.202 g, 26.2 mmol) was then added and the reaction mixture was warmed to RT and stirred for 21 h. The resulting mixture was evaporated under reduced pressure and the solid residue was triturated with a mixture of hexane/EtOAc/Et2O (5/1/1). The solid was collected by filtration, washed and dried under reduced pressure to give 2.56 g of 1-(2-methylsulfanyl-pyrimidin-4-yl)-4-nitro-1H-indole which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399462B2
Source datasetuspto-grants-2013_03
ORD IDord-5c22413d67574e5d8c1a7a09bea04414
Source noteuspto-grants-2013_03