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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68751Generated: October 25, 2026

4-(3-Methylsulfanyl-1-m-tolyl-1H-indazol-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester → 3-Methylsulfanyl-6-(1,2,3,6-tetrahydro-pyridin-4-yl)-1-m-tolyl-1H-indazole

https://huagongshe.com/reaction/68751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Methylsulfanyl-1-m-tolyl-1H-indazol-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl esterHCID 67448865—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product3-Methylsulfanyl-6-(1,2,3,6-tetrahydro-pyridin-4-yl)-1-m-tolyl-1H-indazoleHCID 53494135—

Reaction Steps

A solution of 4-(3-methylsulfanyl-1-m-tolyl-1H-indazol-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (22.5 mg, 0.052 mmol) in 4 N HCl in 1,4-dioxane (3 mL) was stirred at room temperature for 1 h, then concentrated. The resulting residue was triturated and sonicated in a mixture of MeOH (0.5 mL)/diethyl ether (5 mL). The resulting mixture was filtered to yield the title compound as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822447B2
Source datasetuspto-grants-2014_09
ORD IDord-90154f28da444a989d659fbb177a7ff0
Source noteuspto-grants-2014_09