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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611639Generated: October 29, 2026

2-Naphthalenethiol → HCID 178418688, compound

https://huagongshe.com/reaction/1611639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenethiolHCID 7058—
ReactantTriethylamineHCID 8471—
ReactantHCID 178418938HCID 178418938—
Solventtert-ButanolHCID 6386—
ProductHCID 178418688HCID 178418688—

Reaction Steps

To a solution of (5-cyclopropyl-2H-pyrazol-3-yl)-(2,6-dichloropyrimidin-4-yl)-amine (211 mg, 0.781 mmol) and 2-naphthalenethiol (125 mg, 0.781 mmol) in tert-butanol (5 mL) was added triethylamine (174 μL, 1.25 mmol) and the resulting mixture was heated at reflux for 15 hours. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and aqueous NaHCO3. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, Hexane/AcOEt gradient) to afford [6-chloro-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-cyclopropyl-2H-pyrazol-3-yl)-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989385B2
Source datasetuspto-grants-2006_01
ORD IDord-8616291b6a75433387c96792196e8531
Source noteuspto-grants-2006_01