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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47688Generated: October 26, 2026

Sodium Hydroxide → 4-{(2R)-2-[({(2S)-2-hydroxy-3-[4-(2-methoxyethyl)phenoxy]propyl}amino)methyl]-3,4-dihydro-2H-chromen-6-yl}benzoic Acid

https://huagongshe.com/reaction/47688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 4-[(2R)-2-(aminomethyl)-3,4-dihydro-2H-chromen-6-yl]benzoateHCID 9902206—
Reactant(S)-3-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropaneHCID 10976684—
Solvent1,4-DioxaneHCID 31275—
Product4-{(2R)-2-[({(2S)-2-hydroxy-3-[4-(2-methoxyethyl)phenoxy]propyl}amino)methyl]-3,4-dihydro-2H-chromen-6-yl}benzoic AcidHCID 987024210.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of epoxide (Example 16, 0.25 mmol) in 2 mL of aqueous 1,4-dioxane (10% water) was added methyl 4-[(2R)-2-(aminomethyl)-3,4-dihydro-2H-chromen-6-yl]benzoate (40 mg, 0.13 mmol). The mixture was stirred at 80° C. for 72 hours and allowed to cool to room temperature. When ambient temperature was achieved, 1N aqueous sodium hydroxide (1 mL) was added to the solution at room temperature, and stirring continued for another 0.5 hour. The product was then purified by preparative HPLC (Gradient 0-70% Acetonitrile/0.1% aq. TFA) to obtain 6.7 mg of product (as a TFA salt). MH+492.4 (free base).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699860B2
Source datasetuspto-grants-2004_03
ORD IDord-0846486d44fd4fddbad2b57d35bc9362
Source noteuspto-grants-2004_03