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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1424954Erstellt: 27. Oktober 2026

Hydrochloric Acid → cis(+/-)-3-(4-{[(Benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/1424954

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktMethyl cis(+/-)-3-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoateHCID 86648495—
LösungsmittelMethanolHCID 887—
Produktcis(+/-)-3-(4-{[(Benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoic acidHCID 86648496—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Methyl cis(±)-3-(4-{[benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)benzoate obtained in Example (42a) (250 mg, 0.63 mmol) was dissolved in methanol (5 mL). A 1 N aqueous sodium hydroxide solution (4 mL) was added, and the mixture was stirred at 70° C. for one hour. The reaction solution was neutralized with 1 N hydrochloric acid, followed by extraction with ethyl acetate. Then, the organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08927588B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-d9fa58e927984c75a689d1369780e011
Quellennotizuspto-grants-2015_01