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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 412677Erstellt: 24. Oktober 2026

Carbamic Acid → ethyl (S)-[1-(2-benzyloxycarbonylaminopropionyl)-piperidin-4-yloxy]-acetate

https://huagongshe.com/de/reaction/412677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbamic AcidHCID 277—
EduktPivaloyl chlorideHCID 62493—
EduktN-carbobenzyloxyalanineHCID 736104—
EduktEthanol hydrochlorideHCID 21887872—
EduktEthyl (piperidin-4-yloxy)-acetate hydrochlorideHCID 71357176—
LösungsmittelWaterHCID 962—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelEthyl AcetateHCID 8857—
Produktethyl (S)-[1-(2-benzyloxycarbonylaminopropionyl)-piperidin-4-yloxy]-acetateHCID 5992322091,9%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

55.8 g (250 mmol) of (S)-2-benzyloxycarbonylaminopropionic acid (obtainable from the corresponding aminocarboxylic acid by protection of the amino function with a benzyloxycarbonyl derivative; Bodansky et al., loc. cit.) were dissolved in 560 ml of ethyl acetate (Fluka) while stirring and under argon, cooled to 0 to 5° C. and treated with 31.0 ml (250 mmol) of pivaloyl chloride (Fluka). 35.0 ml of triethylamine (Fluka) were added dropwise to the light yellowish solution within 30 minutes, with the temperature being held at 0 to 5° C. A white suspension formed. The white precipitate was filtered off through a pre-cooled glass filter (G3) and the filter cake was washed with 140 ml of cold ethyl acetate (0 to 5° C., Fluka). To the combined filtrates, a clear, colourless liquid which contained the anhydride, were added 55.9 g (250 mmol) of ethyl (piperidin-4-yloxy)-acetate hydrochloride (obtainable from the corresponding tert.-butyl compound (Alig et al., loc. cit.) by trans-esterification with ethanol/hydrochloric acid) and 66.6 g (250 mmol) of Na3PO4.3H2O. The white suspension was treated at 5 to 10° C. 500 ml of deionised water within 30 seconds under argon and while stirring vigorously, with the temperature rising to 20° C. The colourless two-phase system was stirred vigorously at 20 to 25° C. for one hour. Subsequently, the aqueous phase was separated and the organic phase was washed with 1M sodium bicarbonate solution and then with 1N aqueous ammonia solution. The organic phase was dried over about 50 g of sodium sulphate, filtered and the filter cake was washed with about 100 ml of ethyl acetate. The combined filtrates were evaporated in a rotary evaporator and the oily residue was taken up with 100 ml of ethanol. The clear solution was evaporated at 50°/20 mbar to give 90.2 g (92 wt. %) of ethyl (S)-[1-(2-benzyloxycarbonylaminopropionyl)-piperidin-4-yloxy]-acetate as a clear, colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06562977B2
Quelldatensatzuspto-grants-2003_05
ORD IDord-d1d4384f44f54634b65921ea212bd1fb
Quellennotizuspto-grants-2003_05