Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264221Generated: October 27, 2026

Diisopropylethylamine → HCID 178508301, compound

https://huagongshe.com/reaction/2264221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
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—
ReactantHCID 178524907HCID 178524907—
SolventDimethylformamideHCID 6228—
ProductHCID 178508301HCID 17850830135.1%

Reaction Steps

A solution of 1H-1,2,4-triazole-3-carboxylic acid (0.072 g, 0.64 mmol), N-[(dimethylamino)(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methylmethanaminium hexafluorophosphate (0.243 g, 0.64 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.205 mL, 1.17 mmol) in DMF (1.5 mL) was stirred for 15 minutes under argon. Finally, 3″-fluoro-3,2′:3′,4″-terpyridine-5′,6′-diamine (Intermediate 1, 0.15 g, 0.53 mmol) in DMF (3 mL) was added and the mixture was stirred at room temperature for 20 hours. The solvent was evaporated and the crude mixture was purified by silica gel flash chromatography (90:10 dichloromethane/methanol) to give the title compound (0.070 g, 35% of yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855202B2
Source datasetuspto-grants-2010_12
ORD IDord-45c0cb46b2ac4f2e8bf97b724828e2d2
Source noteuspto-grants-2010_12