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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587522Generated: November 1, 2026

Methanol → HCID 178419531, compound

https://huagongshe.com/reaction/1587522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
ReactantHCID 178435382HCID 178435382—
SolventDichloromethaneHCID 6344—
ProductHCID 178419531HCID 178419531—

Reaction Steps

5,7-Diethyl-3-methoxy-1-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]-1,6-naphthyridin-2(1H)-one (80 mg) was suspended in dichloromethane (1 ml) and a 1M solution of boron tribromide in dichloromethane (0.5 ml) was added. The mixture was stirred for 16 hours then methanol (3 ml) was added dropwise. The mixture was heated at reflux for 5 minutes and volatile material was then removed by evaporation. The residue was recrystallised from ethanol/ether to give 5,7-diethyl-3-hydroxy-1-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)-methyl]-1,6-naphthyridin-2(1H)-one hydrobromide as a solid (45 mg), m.p. 190°-194° C.; NMR (d6 -DMSO): 1.24(t, 3H), 1.30(t, 3H), 2.92(q, 2H), 3.22(q, 2H), 5.64(s, 2H), 7.07(d, 2H), 7.22(d, 2H), 7.45-7.75(m, 6H); mass spectrum (+ve FAB, methanol/NBA): 453 (M+H)+ ; microanalysis, found: C, 57.1; H, 4.9; N, 14.7%; C26H24N6O2.Hbr.1.5H2O requires: C, 56.7; H, 5.1; N, 15.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217976
Source datasetuspto-grants-1993_06
ORD IDord-0850bb0980d34ae1b2617fd3c566cfa6
Source noteuspto-grants-1993_06