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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020844Generated: October 31, 2026

N'-(4-benzyloxy-3-cyano-pyridin-2-yl)-2-cyclopropylacetohydrazide → 7-Chloro-3-(cyclopropylmethyl)[1,2,4]triazolo[4,3-a]pyridine-8-carbonitrile

https://huagongshe.com/reaction/1020844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-(4-benzyloxy-3-cyano-pyridin-2-yl)-2-cyclopropylacetohydrazideHCID 66784643—
ReactantHCID 178479711HCID 178479711—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product7-Chloro-3-(cyclopropylmethyl)[1,2,4]triazolo[4,3-a]pyridine-8-carbonitrileHCID 5745959364.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

Intermediate compound D4 (1.4 g, 4.343 mmol) and phosphorous (V) oxychloride (0.810 ml, 8.686 mmol) in DCE (15 ml) were subjected to microwave heating at 150° C. for 5 min. After cooling, the mixture was diluted with DCM and washed with NaHCO3 (aqueous sat. solution). The organic layer was separated, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography (silica gel; DCM/7M solution of NH3 in MeOH up to 2% as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate compound D5 (0.650 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716480B2
Source datasetuspto-grants-2014_05
ORD IDord-8a1c604bbf544ca99ddcfc41a464a2c9
Source noteuspto-grants-2014_05