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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731327Generated: November 3, 2026

2-Aminopyridine → HCID 20228692, compound

https://huagongshe.com/reaction/1731327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantHCID 15054199HCID 15054199—
SolventEthanolHCID 702—
ProductHCID 20228692HCID 202286927.4%

Reaction Steps

A solution of 5-bromoacetyl-2-benzothiazolinone (3.3 g) and 2-aminopyridine (4.2 g) in ethanol was refluxed for 5 hours and the reaction mixture was evaporated in vacuo. To the residue was added a mixture of water and ethyl acetate and the resulting mixture was acidified to pH 1.0 with 10 % hydrochloric acid. The precipitate was collected by filtration and added to a solution of saturated aqueous sodium bicarbonate. The mixture was stirred for 30 minutes. The precipitate was collected by filtration, washed with water and recrystallized from aqueous ethanol to give 5-(imidazo[1,2-a]pyridin-2-yl)-2-benzothiazolinone (0.24 g). mp>270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621084
Source datasetuspto-grants-1986_11
ORD IDord-1554fd4a7c4f40a1975bf7da255d4b5e
Source noteuspto-grants-1986_11