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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525036Erstellt: 24. Oktober 2026

Disodium 2,3-dihydroxybutanedioate → (S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamate

https://huagongshe.com/de/reaction/525036

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDisodium 2,3-dihydroxybutanedioateHCID 13355—
Edukt4-AminotetrahydropyranHCID 419223—
EduktTrimethylaluminumHCID 16682925—
Edukt(S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylateHCID 86722033—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt(S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamateHCID 86722055—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Tetrahydro-2H-pyran-4-amine (900 microl, 8.69 mmols) was added to a solution of (S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylate (900 mg, 2.89 mmols, preparation 109) in toluene (36 ml). A 2M solution of Trimethyl aluminium in toluene (7 ml, 14.00 mmols) was added and it was stirred at 80° C. overnight. Water (50 ml) and a 0.5M solution of sodium tartrate (25 ml) were added. It was extracted with ethylacetate. The combined organic layers were washed with water and brine. It was dried, filtered and concentrated in vacuum. The title compound was obtained (617 mg, 56%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09340547B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-04de8d8e819c4455b3734c36e5918338
Quellennotizuspto-grants-2016_05