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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352468Generated: October 26, 2026

Phosphorus oxychloride → 5-Chlorotetrazolo[1,5-a][1,8]naphthyridine

https://huagongshe.com/reaction/352468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178515417HCID 178515417—
Product5-Chlorotetrazolo[1,5-a][1,8]naphthyridineHCID 22172723—

Reaction Steps

Tetrazolo[1,5-a][1,8]naphthyridin-5-ol (0.5 g, 2.67 mmole) was suspended in phosphorous oxychloride (10 mL) and heated at reflux for 4 hours. The reaction mixture was concentrated under vacuum and the residue was poured into water. Dichloromethane was added and the aqueous layer was made basic with sodium bicarbonate. The dichloromethane layer was separated, dried over magnesium sulfate, filtered and then concentrated under vacuum. The resulting solid was recrystallized from toluene to provide 0.3 g of 5-chlorotetrazolo[1,5-a][1,8]naphthyridine as a solid, m.p. 229-230° C. (decomposition). Analysis: Calculated for C8H4ClN5: %C, 46.73; %H, 1.96; %N, 34.06; Found: %C, 46.87; %H 1.54; %N, 33.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747040B2
Source datasetuspto-grants-2004_06
ORD IDord-b31a0a08f2544876af25064eb071f949
Source noteuspto-grants-2004_06