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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382845Generated: October 31, 2026

Tetrahydrofurfurylamine → N-{5-[(tetrahydrofuran-2-ylmethyl)amino][1,2,4]triazolo[1,5-a]pyridin-2-yl}nicotinamide

https://huagongshe.com/reaction/2382845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofurfurylamineHCID 253298—
ReactantN-(5-bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)nicotinamideHCID 25212514—
ProductN-{5-[(tetrahydrofuran-2-ylmethyl)amino][1,2,4]triazolo[1,5-a]pyridin-2-yl}nicotinamideHCID 59437469—

Reaction Steps

The title compound was prepared following procedure described for example 30 but starting from N-(5-bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)nicotinamide ((B2), 100 mg; 0.31 mmol; 1.0 eq.) and tetrahydrofurfurylamine (1.0 mL) as a white powder (17 mg, 16%). HPLC, Rt: 1.73 min. (purity 95.5%). LC/MS, M+(ESI): 339.1, M−(ESI): 337.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-a5e33f089df747808c0f6c57b5a9a9e6
Source noteuspto-grants-2012_09