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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189156Generated: October 31, 2026

2,6-Dichloropyridine → 2-(4-(6-Chloropyridin-2-yl)but-3-ynyl)benzo[d]thiazole

https://huagongshe.com/reaction/1189156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichloropyridineHCID 16989—
Reactant2-(But-3-yn-1-yl)-1,3-benzothiazoleHCID 57053628—
Product2-(4-(6-Chloropyridin-2-yl)but-3-ynyl)benzo[d]thiazoleHCID 1155114419%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 108(C), from 2,6-dichloro-pyridine (395 mg, 2.67 mmol) and 2-but-3-ynyl-benzo[d]thiazole (100 mg, 0.53 mmol, Example 35(A)). The crude residue was purified by flash chromatography (cyclohexane/AcOEt 4:1) to yield 31 mg (0.10 mmol, 19%) of 2-(4-(6-chloropyridin-2-yl)but-3-ynyl)benzo[d]thiazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-c2f10f96399d40c4aff8804efd753f53
Source noteuspto-grants-2014_03