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HRID 652346Erstellt: 24. Oktober 2026

Sodium Iodide → (3S)-1-[N-[3-[[(t-Butyloxy)carbonyl]amino]-2-oxo-4-phenylbutyl]-N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-proline, t-butyl ester

https://huagongshe.com/de/reaction/652346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktBenzyl chloroformateHCID 10387—
EduktSodium BicarbonateHCID 516892—
Edukttert-Butyl L-alanyl-L-prolinateHCID 12939800—
EduktN-[(t-Butyloxy)carbonyl]-L-phenylalanine chloromethyl ketoneHCID 88667995—
LösungsmittelDimethylformamideHCID 6228—
Produkt(3S)-1-[N-[3-[[(t-Butyloxy)carbonyl]amino]-2-oxo-4-phenylbutyl]-N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-proline, t-butyl esterHCID 13171441751,4%

Reaktionsschritte

A solution of L-alanyl-L-proline t-butyl ester (1.0 g, 4.13 mmol), N-[(t-butyloxy)carbonyl]-L-phenylalanine chloromethyl ketone (1.2 g, 4.03 mmol), sodium bicarbonate (370 mg, 4.4 mmol) and sodium iodide (300 mg, 2 mmol) in dimethylformamide (7 ml) was stirred overnight at room temperature. The reaction mixture was evaporated. Dioxane (6 ml) was added to the residue followed by benzyloxycarbonyl chloride (0.75 ml, 5.24 mmol) and sodium bicarbonate (500 mg, 5.95 mmol). After stirring overnight, the reaction mixture was evaporated, the residue taken up in ethyl acetate and washed neutral (water, saturated sodium bicarbonate solution, water, 10% potassium bisulfate solution and water). The crude material (2.6 g) was chromatographed over silica gel (200 g) using the solvent system ethyl acetate:benzene-1:3 to obtain 1.32 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04670541
Quelldatensatzuspto-grants-1987_06
ORD IDord-d770e609b9924213b201fbf0c6f09e4d
Quellennotizuspto-grants-1987_06