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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252846Generated: October 31, 2026

Ammonia → 1-(3-Bromo-4-ethyl-anilino)-4-[2-(2-chloro-pyridin-4-yl)ethyl]-isoquinoline

https://huagongshe.com/reaction/2252846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178436568HCID 178436568—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product1-(3-Bromo-4-ethyl-anilino)-4-[2-(2-chloro-pyridin-4-yl)ethyl]-isoquinolineHCID 17948432—

Reaction Conditions

Temperature65 °C

Reaction Steps

Under a N2 atmosphere, 150 mg (0.334 mmol) of 1-(3-bromo-4-ethyl-anilino)-4-[2-(2-hydroxy-pyridin-4-yl)-ethyl]-isoquinoline (Ex. 32a) in 5 ml of acetonitrile are mixed with 76 μl (0.83 mmol) of phosphorus oxychloride and 0.17 ml (0.68 mmol) of 4 N HCl in dioxane, and stirred at 65° C. A further 76 μl of phosphorus oxychloride is added after 12 h, and stirring continues for 48 h at 65° C. The mixture is cooled to RT, 4 ml of 10% NH3 solution added, and it is partitioned between 3 portions of EtOAc, 2 portions of water and brine. Drying (Na2SO4), concentrating by evaporation and chromatography on silica gel (acetone/methylene chloride 3:2) yield 1-(3-bromo-4-ethyl-anilino)-4-[2-(2-chloro-pyridin-4-yl)ethyl]-isoquinoline; FAB-MS: (M+H)+=466/468; HPLC(gradient20-100) tRef=13.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323474B2
Source datasetuspto-grants-2008_01
ORD IDord-3d9e43ed94b6491d82e3e01468c80a7f
Source noteuspto-grants-2008_01