Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877522Generated: October 26, 2026

Hydrochloric Acid → 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]benzoic acid hydrochloride

https://huagongshe.com/reaction/1877522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]benzoateHCID 67309136—
Solvent1,4-DioxaneHCID 31275—
Product4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]benzoic acid hydrochlorideHCID 67308954—

Reaction Conditions

Temperature100 °C

Reaction Steps

3.49 ml of 1N hydrochloric acid are added to a solution of 340 mg of 2-methylpropan-2-yl 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]benzoate in 6 ml of dioxane. The reaction mixture is heated at 100° C. in a microwave for 2 hours and then concentrated under reduced pressure. The residue is purified by trituration with diisopropyl ether, so as to give 330 mg of 4-[4-(6-cyanopyridin-3-yl)-9H-carbazol-9-yl]-2-[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]benzoic acid hydrochloride in the form of a pale yellow powder, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309721B2
Source datasetuspto-grants-2012_11
ORD IDord-94401c0ca65d45759e533c20ac3af784
Source noteuspto-grants-2012_11