Hydrochloric Acid → N-(3,4-dihydroxyphenethyl)-2-(3,4-dihydroxyphenyl)-2-hydroxyacetamide

2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid (300 mg, 1.63 mmol) and N-hydroxysuccinimide (188 mg, 1.63 mmol) were dissolved in 1,4-dioxane (20 ml) under nitrogen, and N,N′-dicyclohexylcarbodiimide (336 mg, 1.63 mmol) was added to the mixture at room temperature, which was stirred at this temperature for 16 h. The by-product which precipitated out was filtered off, and the filtrate was added to a solution of 2-(3,4-dihydroxyphenyl)ethylamine hydrochloride (309 mg, 1.63 mmol) in water (20 ml). Sodium hydrogencarbonate (151 mg, 1.8 mmol) was also added, and the reaction mixture was stirred under nitrogen at 50° C. for 1.5 h. The mixture was rendered acidic using 5% strength hydrochloric acid and extracted 3 times with ethyl acetate (a total of 90 ml). The organic phase was washed with saturated NaCl solution, dried over Na2SO4 and filtered, and the filtrate was evaporated under reduced pressure. The product was purified by chromatography on silica gel using the eluent ethyl acetate. The yield was 266 mg of a colorless syrup (51% of theory based on the acid used).

1. customThe by-product which precipitated out
2. filtrationwas filtered off
3. stirringthe reaction mixture was stirred under nitrogen at 50° C. for 1.5 h
4. extractionextracted 3 times with ethyl acetate (a total of 90 ml)
5. washThe organic phase was washed with saturated NaCl solution
6. dry with materialdried over Na2SO4
7. filtrationfiltered
8. customthe filtrate was evaporated under reduced pressure
9. customThe product was purified by chromatography on silica gel using the eluent ethyl acetate

ORDレコード

ord-752eb719072e47dc8f7bd6dcb8c146fd

出典データセット

uspto-grants-2001_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06265611B1