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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254885Generated: October 31, 2026

Hydrochloric Acid → HCID 178428429, compound

https://huagongshe.com/reaction/2254885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 19742893HCID 19742893—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 178428429HCID 178428429—

Reaction Steps

Concentrated hydrochloric acid (0.5 ml) was added to a suspension of 2,6-dimethyl-3-iodo-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methylamino]pyridine (A) (215 mg) in dichloromethane/methanol (4 ml) (1:3 v/v) and the mixture stirred for 30 minutes. Volatile material was removed by evaporation and the residue purified by recrystallisation from methanol to give 2,6-dimethyl-3-iodo-4-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methylamino]pyridine hydrochloride as a white solid, m.p. 238°-240° C. (decomposition); NMR (d6 -DMSO): 2.4(s,3H), 2.7(s,3H), 4.7(d,2H), 6.6(s,1H), 7.1(d,2H), 7.3(d,2H), 7.4-7.7(m,4H), 8.0(t,1H); mass spectrum (positive fast atom bombardment (+ve FAB), DMSO/nitrobenzyl alcohol): 483(M+H)+ ; microanalysis, found: C,48.1; H,4.1; N,16.1%; C21H19N6I.HCl requires: C,48.6; H,3.9; N,16.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236937
Source datasetuspto-grants-1993_08
ORD IDord-d9f8a469c7764011b07caef9050f9035
Source noteuspto-grants-1993_08