Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35217Erstellt: 24. Oktober 2026

Ammonia → 3-(9,10-Didehydro-12-ethylamino-6-methyl-8alpha-ergolinyl)-1,1-diethylurea

https://huagongshe.com/de/reaction/35217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktHydrochloric AcidHCID 313—
Edukt2,3-Dihydroxybutanedioic AcidHCID 875—
EduktDiisobutylaluminumhydrideHCID 21225700—
Edukt3-(12-Acetylamino-9,10-didehydro-6-methyl-8alpha-ergolinyl)-1,1-diethylureaHCID 86742356—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-(9,10-Didehydro-12-ethylamino-6-methyl-8alpha-ergolinyl)-1,1-diethylureaHCID 8674235570%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

200 mg of 3-(12-acetylamino-9,10-didehydro-6-methyl-8α-ergolinyl)-1,1-diethylurea is dissolved in 10 ml of dioxane, combined with 2 ml of 20% diisobutyl aluminum hydride solution in toluene, and heated to 100° C. for 7 hours. The mixture is allowed to cool, then, under cooling, first water, thereafter 2N hydrochloric acid are added thereto, and the solution is rendered alkaline with dilute ammonia, after adding about 1 g of tartaric acid. The mixture is extracted by shaking with methylene chloride, the organic phase is dried and evaporated. The residue is charomatographed as disclosed in Example 7, thus producing 135 mg of 3-(9,10-didehydro-12-ethylamino-6-methyl-8α-ergolinyl)-1,1-diethylurea.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04766128
Quelldatensatzuspto-grants-1988_08
ORD IDord-5ab883efae4c44dbb6f8600b043a3b98
Quellennotizuspto-grants-1988_08