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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640448Generated: October 29, 2026

Tetrahydrofuran → HCID 59255302, compound

https://huagongshe.com/reaction/640448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant3-Ethynylpyridine-2,6-diamineHCID 55281676—
Reactant(6-Phenylsulfanyl-pyridin-3-yl)acetohydroximoyl chlorideHCID 72262849—
SolventWaterHCID 962—
ProductHCID 59255302HCID 5925530258%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a tetrahydrofuran (4 mL) solution of the (6-phenylsulfanyl-pyridin-3-yl)-acetohydroximoyl chloride (100 mg, 0.359 mmol) described in Manufacturing Example 97-1-4 and 3-ethynyl-pyridin-2,6-diamine (15 mg, 0.13 mmol) described in Manufacturing Example 13-1-3 was added triethylamine (55 μL, 0.40 mmol), which was stirred under nitrogen atmosphere for 1 hour at 50° C. Water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:methanol=10:1) to obtain the title compound (25 mg, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-50c1fabdb0a84983a3dc8f7edcd568f0
Source noteuspto-grants-2010_04