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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912775Generated: November 2, 2026

[2-(1-{4-[3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido]phenyl}-1H-indol-4-yloxy)ethyl]-methylcarbamic acid tert-butyl ester → 1-(4-Chloro-3-(tri-fluoromethyl)phenyl)-3-{4-[4-(2-methylamino-ethoxy)-indol-1-yl]phenyl}urea hydrochloride

https://huagongshe.com/reaction/1912775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(1-{4-[3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido]phenyl}-1H-indol-4-yloxy)ethyl]-methylcarbamic acid tert-butyl esterHCID 59725986—
SolventHydrogen chloride-ethyl acetateHCID 21866389—
Product1-(4-Chloro-3-(tri-fluoromethyl)phenyl)-3-{4-[4-(2-methylamino-ethoxy)-indol-1-yl]phenyl}urea hydrochlorideHCID 23154964123.6%

Reaction Steps

In 5 ml of a 4N hydrogen chloride ethyl acetate solution, 200 mg (0.33 mmol) of [2-(1-{4-[3-(4-chloro-3-(trifluoromethyl)phenyl)ureido]phenyl}-1H-indol-4-yloxy)ethyl]-methylcarbamic acid tert-butyl ester was dissolved and the solution was stirred at room temperature for 14 hours. The reaction solution was concentrated under reduced pressure, and then the obtained residue was triturated with ethyl acetate to obtain 110 mg (66%) of 1-(4-chloro-3-(tri-fluoromethyl)phenyl)-3-{4-[4-(2-methylamino-ethoxy)-indol-1-yl]phenyl}urea hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-fca6edf41bc14396a456c78aecfba7c2
Source noteuspto-grants-2013_12