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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640536Generated: November 1, 2026

Triethylamine → HCID 59255245, compound

https://huagongshe.com/reaction/640536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Ethynylpyridin-2-amineHCID 12422526—
Reactant(6-Benzyl-pyridin-3-yl)-acetohydroximoyl chlorideHCID 72262889—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59255245HCID 592552455.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-ethynyl-pyridin-2-ylamine (30 mg, 0.25 mmol) described in Manufacturing Example 1-2-3, 2-(6-benzyl-pyridin-3-yl)-acetohydroximoyl chloride (88 mg, 0.34 mmol) described in Manufacturing Example 210-1-7, triethylamine (77 mg, 0.76 mmol), and tetrahydrofuran (5 mL) was stirred for 25 minutes at 50° C. This reaction solution was partitioned into ethyl acetate and water. The organic layer was separated and concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=2:1, 1:1, ethyl acetate) to obtain the title compound (4.6 mg, 5.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-8c767eb04a764466a014fc9174a5a010
Source noteuspto-grants-2010_04