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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008102Generated: November 1, 2026

Propargyl bromide → HCID 21913055, compound

https://huagongshe.com/reaction/1008102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
Reactant(3-Bromoprop-1-yn-1-yl)benzeneHCID 10987157—
ReactantHCID 21913508HCID 21913508—
ProductHCID 21913055HCID 21913055—

Reaction Steps

The general method described in Part A of Example 81 was followed, using 2-(8-ethoxymethyl-5,6-dimethyl-7H-imidazo [4,5-c]tetrazolo [1,5-a]pyridin-7-yl)ethanol (4.51 g, 15.5 mmol) in lieu of tert-butyl 2-hydroxyethylcarbamate and 3-bromo-1-phenylpropyne, prepared as described in Part A of Example 7, in lieu of propargyl bromide. The crude product was triturated with diethyl ether, isolated by filtration, and dried under reduced pressure to provide 5.93 g of 8-ethoxymethyl-5,6-dimethyl-7-{2-[(3-phenylprop-2-ynyl)oxy]ethyl}-7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797718B2
Source datasetuspto-grants-2004_09
ORD IDord-d3f79878b76d41899d46562c4bd81ac0
Source noteuspto-grants-2004_09