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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487947Generated: October 26, 2026

5-(Piperidin-4-YL)-1H-indazole → (4-Cyclobutyl-2-methyl-5-(5-methyl-4H-1,2,4-triazol-3-yl)phenyl)(4-(imidazo[1,2-a]pyridin-6-yl)piperidin-1-yl)methanone

https://huagongshe.com/reaction/1487947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Piperidin-4-YL)-1H-indazoleHCID 49760859—
Reactant4-Cyclobutyl-2-methyl-5-(methylcarbamoyl)benzoic acidHCID 90022051—
Reactant6-(Piperidin-4-yl)imidazo[1,2-a]pyridine hydrochlorideHCID 90030382—
ReactantHCID 178433965HCID 178433965—
Product(4-Cyclobutyl-2-methyl-5-(5-methyl-4H-1,2,4-triazol-3-yl)phenyl)(4-(imidazo[1,2-a]pyridin-6-yl)piperidin-1-yl)methanoneHCID 178433959—

Reaction Steps

The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 62, except 4-cyclobutyl-2-methyl-5-(5-methyl-4H-1,2,4-triazol-3-yl)benzoic acid (compound 78.4, 100 mg) was used in place of 4-cyclobutyl-2-methyl-5-(methylcarbamoyl)benzoic acid (compound 62.3) and 6-(piperidin-4-yl)imidazo[1,2-a]pyridine hydrochloride (compound 78.5, 88 mg) was used in place of 5-(piperidin-4-yl)-1H-indazole (compound 62.5). The title compound was obtained as a white solid (35.6 mg, 21%). m/z (ES+) 455 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-474b15452321455f916bc2b9fb33db91
Source noteuspto-grants-2016_08