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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346321Erstellt: 23. Oktober 2026

Ammonia → 1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine

https://huagongshe.com/de/reaction/346321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktSodium CarbonateHCID 10340—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt1H-Pyrrole, 1-benzoyl-2,5-dihydro-HCID 11252283—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidineHCID 70282017—

Reaktionsschritte

41.5 g (0.24 mol) of 1-benzoyl-2,5-dihydropyrrole are initially introduced into 240 ml of methylene chloride, and 24.8 g (0.3 mol) of methanesulphonyl chloride are added dropwise at 0° C. The mixture is subsequently stirred at room temperature for 16 hours, the solvent is then stripped off under 8 mbar and the residue is taken up in 240 ml of tetrahydrofuran. After addition of 65 g of 25% strength ammonia solution, the mixture is heated at 80° C. in an autoclave for 10 hours. It is then poured into 5 times the amount of water, the pH is brought to 10-11 with sodium carbonate, the mixture is extracted with methylene chloride and the extract is dried over sodium sulphate and concentrated. The crude product (50 g) is chromatographed on silica gel (mobile phase initially ethanol:ethyl acetate 1:3, then ethanol; Rf value: 0.34 ethanol). Yield: 33.5 g (59% of theory).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05061712
Quelldatensatzuspto-grants-1991_10
ORD IDord-0261170fe1524559b435f9b568c4bc3a
Quellennotizuspto-grants-1991_10