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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541280Generated: October 31, 2026

4-(Piperidin-4-yl)benzonitrile--hydrogen chloride (1/1) → HCID 178494837, compound

https://huagongshe.com/reaction/541280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Piperidin-4-yl)benzonitrile--hydrogen chloride (1/1)HCID 19391618—
Reactant4-(4-(Trifluoromethyl)phenyl)piperidine hydrochlorideHCID 45073796—
ReactantHCID 178494838HCID 178494838—
ProductHCID 178494837HCID 178494837—

Reaction Steps

The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of 4-(1-(4-cyclobutyl-5-(5-(2-methoxyethyl)-4H-1,2,4-triazol-3-yl)-2-methylbenzoyl)piperidin-4-yl)benzonitrile (compound 153), using 4-(4-(trifluoromethyl)phenyl)piperidine hydrochloride salt instead of 4-(piperidin-4-yl)benzonitrile hydrochloride salt (compound 1.5). m/z (ES+) 527 (M+H)+. 1H NMR (400 MHz, Chloroform-d) δ 11.30-11.10 (br, 1H), 7.60-7.47 (m, 3H), 7.35-7.28 (m, 3H), 5.10-4.93 (m, 1H), 4.24-4.13 (m, 1H), 3.78 (t, 2H), 3.70 (d, 1H), 3.45 (s, 3H), 3.12 t, 2H), 3.15-3.05 (m, 1H), 2.90-2.75 (m, 2H), 2.44 and 2.35 (2 singlets, amide rotamers, ArCH3, 3H), 2.25-2.13 (m, 2H), 2.13-1.85 (m, 4H), 1.87-1.66 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-a9e2b40203294d21924d0fcb322caaf0
Source noteuspto-grants-2014_10