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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33420Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/33420

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
PatentnummerUS07429587B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-5eb15583d29d4596b2376fa164d946a4
Quellennotizuspto-grants-2008_09