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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2370534Erstellt: 23. Oktober 2026

Diisopropylethylamine → (S)-tert-butyl 3-(6-(2-chloropyridin-4-yloxy)benzo[d]thiazol-2-ylamino)piperidine-1-carboxylate

https://huagongshe.com/de/reaction/2370534

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
Edukt6-(2-Chloropyridin-4-yloxy)-2-(methylsulfinyl)benzo[d]thiazoleHCID 57725430—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt(S)-tert-butyl 3-(6-(2-chloropyridin-4-yloxy)benzo[d]thiazol-2-ylamino)piperidine-1-carboxylateHCID 57725807112%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

To the solution of 6-(2-chloropyridin-4-yloxy)-2-(methylsulfinyl)benzo[d]thiazole (100 mg, 0.31 mmol) in 1.6 ml of NMP was added (S)-tert-butyl 3-aminopiperidine-1-carboxylate (200 mg, 1 mmol) and DIPEA (70 μL, 0.4 mmol). The reaction solution was stirred at 95° C. for 5 days. The crude reaction solution was purified on prep HPLC and evaporated in vaccuo to give (S)-tert-butyl 3-(6-(2-chloropyridin-4-yloxy)benzo[d]thiazol-2-ylamino)piperidine-1-carboxylate (160 mg) as TFA salt. ES/MS m/z 461.1 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08710048B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-54e39376a176469aa5db12fd22dbd2de
Quellennotizuspto-grants-2014_04