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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82734Generated: October 30, 2026

Phosphorus pentachloride → HCID 67436031, compound

https://huagongshe.com/reaction/82734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-cyano-N-{4-[4-(3-cyano-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-yl}benzamideHCID 67435694—
SolventBenzeneHCID 241—
ProductHCID 67436031HCID 67436031—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 3-cyano-N-{4-[4-(3-cyano-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-yl}benzamide (30 mg, 72 μmol) in benzene (2 mL) at 0° C. was treated with phosphorus pentachloride (45 mg, 0.22 mmol) and stirred at 90° C. for 2 h. The reaction mixture was concentrated, diluted with ethanol (2.5 mL), treated with sodium cyanoborohydride (14 mg, 0.22 mmol), and stirred for 16 h. The reaction mixture was purified by preparative LCMS to give the intermediate 5-[3-{4-[(3-cyanobenzyl)amino]-1,2,5-oxadiazol-3-yl}-5-oxo-1,2,4-oxadiazol-4(5H)-yl]-2-fluorobenzonitrile. This material was diluted with ethanol (1 mL), treated with 2.0 M sodium hydroxide in water (0.2 mL), and stirred for 45 min. Purification of the crude reaction mixture by preparative HPLC gave the desired product (3 mg, 11%). LCMS for C18H13FN7O2 (M+H)+: m/z=378.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846726B2
Source datasetuspto-grants-2014_09
ORD IDord-3a541b32effe448993e34552296777c4
Source noteuspto-grants-2014_09