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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264214Generated: November 1, 2026

Diisopropylethylamine → HCID 68787687, compound

https://huagongshe.com/reaction/2264214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Chloropyridine-4-carboxylic acidHCID 2735816—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3''-Fluoro-3,2':3',4''-terpyridine-5',6'-diamineHCID 59595954—
SolventDimethylformamideHCID 6228—
ProductHCID 68787687HCID 68787687—

Reaction Steps

A solution of 3-chloroisonicotinic acid (0.075 g, 0.48 mmol), N—[(dimethylamino)(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methylmethanaminium hexafluorophosphate (0.178 g, 0.47 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.15 mL, 0.86 mmol) in DMF (1 mL) was stirred 15 minutes. Finally, 3″-fluoro-3,2′:3′,4″-terpyridine-5′,6′-diamine (Intermediate 1, 0.11 g, 0.39 mmol) in DMF (2.9 mL) was added and the mixture was stirred at room temperature 3.5 hours. The crude mixture was extracted between ethyl acetate and water. The organic layer was washed with water and brine, dried (MgSO4) and evaporated. The residue (0.195 g) was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855202B2
Source datasetuspto-grants-2010_12
ORD IDord-ab6d5a93499042cd942e142ef0017da9
Source noteuspto-grants-2010_12