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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987330Generated: October 29, 2026

Sodium Bicarbonate → HCID 69629173, compound

https://huagongshe.com/reaction/987330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-Isocyanato-4-[(trifluoromethyl)sulfanyl]benzeneHCID 2733392—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 86595065HCID 86595065—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69629173HCID 6962917357%

Reaction Steps

3-{4-[2-(4-Aminophenyl)ethoxy]phenyl}-(S)-2-ethoxypropanoic acid hydro chloride (described in Example 56a) (0.2 g; (0.547 mmole) was dissolved in tetrahydrofuran (5 ml). Sodium hydrogencarbonate (0.051 g; 0.607 mmole) was added and the mixture was stirred for a little while. 4-(Trifluoromethylthio)phenyl isocyanate (0.126 g; 0.575 mmole) was added. The reaction mixture was stirred at room temperature for 6 hours and then evaporated to dryness. Ethyl acetate and water were added to the residue and the phases were separated. The organic phase was dried with magnesium sulfate and the solvent was evaporated. Chromatography of residue on silica gel (isolute, SI) using dichloromethane, methanol:dichloromethane (1:99) and then methanol:dichloromethane (2:98) as eluants gave 0.17 g (57% yield) of (S)-2-ethoxy-3-[4-(2-{4-[({4-[(trifluoromethyl)sulfanyl]anilino}carbonyl)amino]phenyl}ethoxy)phenyl]propanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630600B1
Source datasetuspto-grants-2003_10
ORD IDord-e3ee2f4384b94cd4ab8f38750f0d97a0
Source noteuspto-grants-2003_10