Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541263Generated: October 31, 2026

2-(Tetrahydrofuran-3-yl)acetohydrazide → HCID 178424706, compound

https://huagongshe.com/reaction/541263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tetrahydrofuran-3-yl)acetohydrazideHCID 68288816—
ReactantHCID 86672529HCID 86672529—
Reactant4-(1-(2,4-dimethyl-5-(5-((tetrahydrofuran-3-yl)methyl)-4H-1,2,4-triazol-3-yl)benzoyl)piperidin-4-yl)benzonitrileHCID 178424704—
ProductHCID 178424706HCID 178424706—

Reaction Steps

The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of 4-(1-(2,4-dimethyl-5-(5-((tetrahydrofuran-3-yl)methyl)-4H-1,2,4-triazol-3-yl)benzoyl)piperidin-4-yl)benzonitrile (compound 130), using 3-cyanopropanehydrazide (compound 140.1) instead of 2-(tetrahydrofuran-3-yl)acetohydrazide (compound 130.4). m/z (ES+) 439 (M+H)+. 1H-NMR (300 Hz, CD3OD): δ 7.68 (d, 2H), 7.58-4.47 (m, 3H), 7.30 (s, 1H), 4.89-4.80 (m, 1H), 3.65-3.62 (m, 1H), 3.32-3.30 (m, 1H), 3.15 (t, 2H), 3.03-2.95 (m, 4H), 2.50 (s, 3H), 2.42 and 2.32 (2 singlets, amide rotamers, ArCH3, 3H), 2.03-2.00 (m, 1H), 1.83-1.78 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-29fa153990d747de801e47e6d0f545b8
Source noteuspto-grants-2014_10