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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 523649Erstellt: 24. Oktober 2026

Diisopropylethylamine → (R)-3-tert-Butoxy-2-[(1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-amino]-propionic acid tert-butyl ester

https://huagongshe.com/de/reaction/523649

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-Chloro-4-hydroxyisoquinoline-3-carboxylic acidHCID 11020520—
EduktH-D-Ser(tBu)-OtBu.HClHCID 56777372—
EduktHCID 178484681HCID 178484681—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-3-tert-Butoxy-2-[(1-chloro-4-hydroxy-isoquinoline-3-carbonyl)-amino]-propionic acid tert-butyl esterHCID 8659544731,9%

Reaktionsschritte

To a mixture of 45 mg (0.2 mmol) of 1-chloro-4-hydroxy-isoquinoline-3-carboxylic acid, 76 mg (0.2 mmol) of benzotriazol-1-yl-(bis-dimethylamino-methylene)-oxonium hexafluoro phosphate (HBTU), 50.8 mg (R)-2-amino-3-tert-butoxy-propionic acid tert-butyl ester hydrochloride (0.2 mmol), and 1 ml of dichloromethane was added 122.5 μl (0.7 mmol) of ethyl-diisopropyl-amine with stirring. Stirring was continued at ambient temperature for 40 h. The product was isolated from the reaction mixture by flash column chromatography on silica gel using hexanes:ethyl acetate (9:1) as the eluent to give a colorless oil. 27 mg of the title compound was obtained; MS-(+)-ion: M+1=422.8 amu.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09339527B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-c3bb4497bfa741edbcfea147cf4d5a21
Quellennotizuspto-grants-2016_05