Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636751Generated: October 29, 2026

Ro 48-8071 → HCID 18434102, compound

https://huagongshe.com/reaction/1636751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRo 48-8071HCID 1949—
ReactantPotassium CarbonateHCID 11430—
Reactant4-MethoxybenzylamineHCID 75452—
SolventTolueneHCID 1140—
ProductHCID 18434102HCID 18434102—

Reaction Steps

Analogously to Example 33, 17.55 g of [4-[6-(allyl-methyl-amino)-hexyloxy]-2-fluoro-phenyl]-(4-bromo-phenyl)-methanone are boiled under reflux for 23 hrs. with 50.7 ml of 4-methoxy-benzylamine and 6.5 g of potassium carbonate in 600 ml of toluene. After filtration, evaporation and purification over silica gel with methylene chloride/methanol (2.5% to 10%) there are obtained 17.43 g of [4-[6-(allyl-methyl-amino)-hexyloxy]-2-(4-methoxy-benzylamino)-phenyl]-(4-bromo-phenyl)-methanone. A solution of this material in 200 ml of trifluoroacetic acid is stirred at room temperature for 45 hrs., evaporated and the residue is converted into the free base with methylene chloride/saturated sodium bicarbonate solution. After purification over silica gel with methylene chloride/methanol (9:1) there are obtained 13.23 g of [2-amino-4-[6-(allyl-methyl-amino)-hexyloxy]-phenyl]-(4-bromo-phenyl)-methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034275
Source datasetuspto-grants-2000_03
ORD IDord-b0b6f8706cd64107a5c15717caea178e
Source noteuspto-grants-2000_03