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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723233Generated: November 1, 2026

Hydrochloric Acid → HCID 178526907, compound

https://huagongshe.com/reaction/1723233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantSodium AzideHCID 33557—
Reactant3-(4-Cyano-2-methoxybenzyl)1-methyl-5-nitroindoleHCID 23365877—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178488254HCID 178488254—
ProductHCID 178526907HCID 178526907590.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 3-(4-cyano-2-methoxybenzyl)-1-methyl-5-nitroindole (0.458 g.), sodium azide (0.741 g.), and triethylamine hydrochloride (0.785 g.) in dry N-methyl-2-pyrrolidinone (6 ml.), under nitrogen, was stirred and heated at 150° C. for 1.5 hours. The mixture was cooled to ambient temperature, 1N hydrochloric acid (25 ml.) added cautiously, while stirring, the precipitated solid isolated by filtration, washed with water and dried in vacuo to give 3-[2-methoxy-4-(1-H-tetrazol-5-yl)benzyl]-1-methyl-5-nitroindole, (V) (0.484 g., 94%) as a yellow powder, m.p. 249°-250° C. partial NMR (250 MHz, DMSO-d6): 3.82 (s,3H, NMe); 3.97(s,3H, OMe); 4.13(s,2H, ArCH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859692
Source datasetuspto-grants-1989_08
ORD IDord-6384765200e9494e961686002dba133f
Source noteuspto-grants-1989_08