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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7272Erstellt: 23. Oktober 2026

L-Methionine → tert-Butyl N-[(benzyloxy)carbonyl]-L-methionyl-L-alaninate

https://huagongshe.com/de/reaction/7272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-MethionineHCID 6137—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktL-Alanine 1,1-dimethylethyl esterHCID 89016—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTriethylamineHCID 8471—
Produkttert-Butyl N-[(benzyloxy)carbonyl]-L-methionyl-L-alaninateHCID 16124765109,3%

Reaktionsschritte

Z-Protected L-methionine (10 g) was dissolved in DMF (200 ml) and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (8.13 g) was added followed by HOBT (5.72 g) and triethylamine (19.7 ml). The mixture was stirred for 1 h then L-alanine tert-butyl ester (7.7 g) was added and stirring continued for 18 h. The mixture was concentrated under reduced pressure and partitioned between diethyl ether and water. The separated organic phase was washed with hydrochloric acid (1M), saturated sodium bicarbonate solution and brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (11.9 g) as an orange oil which crystallised on standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084139B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-acb43fa5eb1b42d09e33b5d59c24f091
Quellennotizuspto-grants-2006_08