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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878251Generated: November 1, 2026

Ammonium Chloride → HCID 70663490, compound

https://huagongshe.com/reaction/878251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 70663556HCID 70663556—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 70663490HCID 70663490—

Reaction Steps

A solution of N-(4-(4-fluoro-2-methoxyphenyl)pyridin-3-yl)-3-mercapto-N-methyl-5-(trifluoromethyl)benzamide (0.065 g, 149 μmol, example 216, intermediate a) in acetonitrile (2 mL) was treated with 1-bromo-2-methoxyethane (24.8 mg, 16.8 μL, 179 μmol) and DIPEA (38.5 mg, 52.0 μL, 298 μmol) and stirred at room temperature for 5 hours. The reaction mixture was poured on saturated aqueous NH4Cl solution and EtOAc and the layers were separated. The aqueous layer was extracted twice with EtOAc. The organic layers were dried over MgSO4, filtered, treated with silica gel and evaporated. The compound was purified by silica gel chromatography on a 10 g column using an MPLC system eluting with a gradient of n-heptane:EtOAc (100:0 to 0:100). Colorless solid (0.04 g; 54%). MS (ESI): m/z=495.14 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987307B2
Source datasetuspto-grants-2015_03
ORD IDord-5b89852c1348412ba36cc7b71be5f8ee
Source noteuspto-grants-2015_03