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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30335Erstellt: 23. Oktober 2026

Potassium Sodium Tartrate → tert-Butyl(3S)-3-({[2-[(aminocarbonyl)amino]-5-(4-methoxyphenyl)-3-thienyl]carbonyl}amino)piperidine-1-carboxylate

https://huagongshe.com/de/reaction/30335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Sodium TartrateHCID 9357—
Edukttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
EduktMethyl 5-(4-methoxyphenyl)-2-({[(trichloroacetyl)amino]carbonyl}amino)thiophene-3-carboxylateHCID 11546916—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl(3S)-3-({[2-[(aminocarbonyl)amino]-5-(4-methoxyphenyl)-3-thienyl]carbonyl}amino)piperidine-1-carboxylateHCID 6927178867%

Reaktionsschritte

To a solution of methyl 5-(4-methoxyphenyl)-2-({[(trichloroacetyl)amino]carbonyl}amino)thiophene-3-carboxylate (1.0 g, 2.2 mmol) in dry THF (20 mL) was added a solution of [Me2Al-3-Boc-(S)-3-aminopiperidine] in THF (which was preformed by the addition of Me3Al (2.0 M in hexanes, 2.2 nL, 4.4 mmol) to a solution of (S)-3-Amino-piperidine-1-carboxylic acid tert-butyl ester (0.89 g, 4.4 mmol) in 10 mL THF at −78° C. followed by warming to room temperature for an additional 15 min). The resulting orange-colored solution was stirred overnight at room temperature. The reaction mixture was cooled with ice and a 10% aqueous solution of Rochelle's salt was added slowly to quench the reaction. The resulting biphasic solution was warmed to room temperature and stirred for an additional 1 h. The mixture was diluted with EtOAc and H2O, the aqueous layer was extracted with EtOAc (3×) and the combined organic extracts were washed with H2O, brine and dried (Na2SO4). Evaporation gave a pale orange solid. Purification by column chromatography (SiO2, 50% EtOAc/hexanes) gave 0.70 g (67%) of a light yellow solid. LC/MS (APCI, ES, M+H=475).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423061B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-d66aea6f837c4ae596788447543f1d0d
Quellennotizuspto-grants-2008_09