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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819425Generated: November 1, 2026

Hydrochloric Acid → HCID 178511543, compound

https://huagongshe.com/reaction/1819425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(2-(Trifluoromethoxy)phenyl)methanamineHCID 2777251—
Reactant{4-[(2-Chloro-5-fluoro-pyrimidin-4-ylamino)-methyl]-cyclohexyl}-carbamic acid tert-butyl esterHCID 59845697—
SolventEthyl AcetateHCID 8857—
ProductHCID 178511543HCID 17851154315%

Reaction Conditions

Temperature180 °C

Reaction Steps

{4-[(2-Chloro-5-fluoro-pyrimidin-4-ylamino)-methyl]-cyclohexyl}-carbamic acid tert-butyl ester (127 mg, 0.35 mmol) was dissolved in 2-trifluoromethoxybenzylamine (2.5 mL) and heated at 180° C. for 20 min. The reaction mixture was diluted with EtOAc and poured into 1N HCl. The aqueous layer was separated and extracted with EtOAc (×2). The combined organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo. The resulting residue was dissolved in CH2Cl2 (2.5 mL) and TFA (2.5 mL) was added. The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was concentrated in vacuo and the resulting residue was diluted with EtOAc. The solution was poured into 10% NaHCO3 and the aqueous layer was re-extracted with EtOAc. The combined organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo. The resulting residue was purified by silica gel preparative TLC using 9:1:0.1 CH2Cl2:MeOH:NH4OH as an eluent to afford 22 mg (15%) of the title compound, m/z 414.6 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601714B2
Source datasetuspto-grants-2009_10
ORD IDord-d46c8db25d8244d09b478ba7109e336c
Source noteuspto-grants-2009_10