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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43843Erstellt: 26. Oktober 2026

tert-Butyl cis(+/-)-4-{[(benzyloxy)carbonyl]amino}-3-(dimethylamino)piperidine-1-carboxylate → tert-Butyl cis(+/-)-4-amino-3-(dimethylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/43843

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl cis(+/-)-4-{[(benzyloxy)carbonyl]amino}-3-(dimethylamino)piperidine-1-carboxylateHCID 86648775—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladium hydroxideHCID 9942167—
LösungsmittelMethanolHCID 887—
Produkttert-Butyl cis(+/-)-4-amino-3-(dimethylamino)piperidine-1-carboxylateHCID 86648776100,3%

Reaktionsschritte

20% Palladium hydroxide (15 mg) was added to a solution of tert-butyl cis(±)-4-{[(benzyloxy)carbonyl]amino}-3-(dimethylamino)piperidine-1-carboxylate obtained in Example (200b) (144 mg, 0.381 mmol) in methanol (4 mL) at room temperature, and the mixture was stirred in a hydrogen atmosphere at 50° C. for six hours. The insoluble matter was separated by filtration, and the filtrate was concentrated under reduced pressure to obtain 93 mg of the title compound (100%) as a colorless oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536197B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-468919df26d0497f9a7888a7987dac19
Quellennotizuspto-grants-2013_09