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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422367Generated: October 27, 2026

2-(6-Bromohex-1-ynyl)pyridine → HCID 66598079, compound

https://huagongshe.com/reaction/422367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(6-Bromohex-1-ynyl)pyridineHCID 20331212—
ReactantHCID 178418385HCID 178418385—
SolventCyclohexane ethylacetateHCID 21867204—
ProductHCID 66598079HCID 6659807913.3%

Reaction Steps

The title compounds were prepared, in accordance with the general method of Example 109(D), from 2-(6-bromo-hex-1-ynyl)-pyridine (250 mg, 1.05 mmol) and benzotriazole (125 mg, 1.05 mmol). The crude product was purified by flash chromatography (cyclohexane/AcOEt 3:2) to yield 2-(6-(pyridin-2-yl)hex-5-ynyl)-2H-benzo[d][1,2,3]triazole (38 mg, 0.14 mmol, 13%) as a brown oil and (cyclohexane/AcOEt 1:1) to yield 1-(6-(pyridin-2-yl)hex-5-ynyl)-1H-benzo[d][1,2,3]triazole (48 mg, 0.17 mmol, 16%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-f849659441cb48ecb77aa1f8cd63d459
Source noteuspto-grants-2012_01