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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192523Generated: November 2, 2026

Diisopropylethylamine → 5-{5-[4-(Ethyloxy)-3,5-difluorophenyl]-1,2,4-oxadiazol-3-yl}isoquinoline

https://huagongshe.com/reaction/2192523

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—
Reactant4-Ethoxy-3,5-difluorobenzoic acidHCID 46737603—
ReactantHCID 178513273HCID 178513273—
SolventDimethylformamideHCID 6228—
Product5-{5-[4-(Ethyloxy)-3,5-difluorophenyl]-1,2,4-oxadiazol-3-yl}isoquinolineHCID 444764915.8%

Reaction Steps

A mixture of 4-(ethyloxy)-3,5-difluorobenzoic acid (JRD Fluorochemicals Ltd; 130 mg, 0.641 mmol), HATU (244 mg, 0.641 mmol), Hunig's base (0.3 mL, 1.718 mmol) in N,N-dimethylformamide (DMF) (1 ml) was stirred at room temperature for 1 hr before the addition of N-hydroxy-5-isoquinolinecarboximidamide (D1; 100 mg, 0.534 mmol) in N,N-dimethylformamide (DMF) (1 ml). The reaction mixture was stirred at room temperature for 2-3 hrs and then heated in a microwave at 140° C. for 1.5 hr. The reaction mixture was concentrated in vacuo and purified by preparative HPLC (Waters Atlantis column, eluting with solvents A/B (A: Water+0.1% Formic acid, B: MeCN+0.1% Formic acid)) to give the title compound (11 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329730B2
Source datasetuspto-grants-2012_12
ORD IDord-86653cf6080a474fb54d01a192077af1
Source noteuspto-grants-2012_12