Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986644Generated: October 31, 2026

HCID 10055409, compound → HCID 10347968, compound

https://huagongshe.com/reaction/1986644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10055409HCID 10055409—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 10347968HCID 1034796885%

Reaction Conditions

Temperature75 °C

Reaction Steps

To N-[2-(5-tert-Butyl-3-methanesulfonylamino-2-methoxy-phenylcarbamoyl)-benzo[b]thiophen-7-yl]-6-(4-methoxy-benzylamino)-nicotinamide (Example 1) (20 mg) in a sealed tube was added 90 μL of trifluoroacetic acid. The clear solution was purged with Ar and then heated to 75° C. in a sealed tube 12 h. The reaction was cooled to room temperature and diluted with toluene to remove excess trifluoroacetic acid in vacuo. The resulting trifluoroacetic acid salt of the desired product was dissolved in EtOAc and washed with saturated NaHCO3 solution and brine. The organics were dried over MgSO4, filtered and concentrated to give a foam which was further purified by flash chromatography on silica gel (7%-10% MeOH/CH2Cl2) to provide the title compound as a white solid (14 mg, 85% yield), m.p. 234-235° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550461B2
Source datasetuspto-grants-2009_06
ORD IDord-d6a2c8dd5f944fc7bdc04f9e0fae8f14
Source noteuspto-grants-2009_06