Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172918Generated: October 26, 2026

1-Hydroxybenzotriazole → 4-[3-(3-Chloro-4-isopropoxy-phenyl)-[1,2,4]oxadiazol-5-yl]-3-methyl-pyridine

https://huagongshe.com/reaction/1172918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantCarbodiimideHCID 160435—
Reactant3-Methyl-isonicotinic acidHCID 1502003—
ReactantHCID 178458441HCID 178458441—
SolventAcetonitrileHCID 6342—
Product4-[3-(3-Chloro-4-isopropoxy-phenyl)-[1,2,4]oxadiazol-5-yl]-3-methyl-pyridineHCID 5955666910.4%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a microwave vial charged with 3-chloro-N-hydroxy-4-isopropoxy-benzamidine (75 mg, 0.328 mmol), 3-methyl-isonicotinic acid (41 mg, 0.298 mmol), HOBt (46 mg, 0.298 mmol), PS-carbodiimide (720 mg, 0.894 mmol, loading 1.24 mmol/g) was added acetonitrile (3.5 mL) and diisopropylethylamine (156 μL, 0.894 mmol). The reaction vial was capped and heated at about 160° C. for about 30 minutes in a Biotage microwave. The reaction mixture was filtered and the resin was washed with acetonitrile (4 mL). Filtrate was concentrated to dryness. The crude product was purified via reverse phase HPLC (30-90% acetonitrile, 30 minute ramp) to give 10.2 mg (10%) of 4-[3-(3-chloro-4-isopropoxy-phenyl)-[1,2,4]oxadiazol-5-yl]-3-methyl-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834039B2
Source datasetuspto-grants-2010_11
ORD IDord-4dc39e01fa6242ba936217e2a406435d
Source noteuspto-grants-2010_11