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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964912Generated: November 3, 2026

4-Toluenesulfonyl chloride → HCID 86646366, compound

https://huagongshe.com/reaction/1964912

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantCyclohexaneHCID 8078—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 58086168HCID 58086168—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86646366HCID 86646366—

Reaction Steps

To (3-nitro-phenyl)-(5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone (536, 291 mg, 0.85 mmol) in tetrahydrofuran (7 mL) was added 1.5 M of lithium diisopropylamide in cyclohexane (676 μl, 1.59 mmol) at −78° C. under an atmosphere of nitrogen. After 30 minutes, p-toluenesulfonyl chloride (209 mg, 1.10 mmol) was added in tetrahydrofuran and the reaction was stirred for three hours. The reaction was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. All solids were filtered and purified by silica gel column chromatography eluting with 60% ethyl acetate in hexane to give the compound (537, 182 mg, 43%). MS(ESI)[M+H+]+=499.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415469B2
Source datasetuspto-grants-2013_04
ORD IDord-dd0ad1a166934cc992c9e6ec9cd89cfb
Source noteuspto-grants-2013_04