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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346945Erstellt: 24. Oktober 2026

Diisopropylethylamine → [4-Cyclopropanesulfonylaminocarbonyl-18-(isoquinolin-1-yloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-en-14-yl]-carbamic acid tetrahydro-furan-3-yl ester

https://huagongshe.com/de/reaction/346945

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktOxolan-3-yl chloroformateHCID 15291007—
EduktHCID 86597622HCID 86597622—
LösungsmittelDichloromethaneHCID 6344—
Produkt[4-Cyclopropanesulfonylaminocarbonyl-18-(isoquinolin-1-yloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-en-14-yl]-carbamic acid tetrahydro-furan-3-yl esterHCID 7242750252,6%

Reaktionsschritte

Prepared from cyclopropanesulfonic acid [14-amino-18-(isoquinolin-1-yloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carbonyl]-amide bis hydrochloride (50 mg, 0.075 mmol), 44 μL (0.25 mmol) of DIPEA and 0.10 mL (0.1 mmol) of tetrahydro-furan-3-yl chloroformate (prepared by treating tetrahydrofuran-3-ol with phosgene) in DCM as described in the procedure above to give 28 mg (52%) of a white solid. Preparative HPLC condition: YMC ODS-A, S5, 30×50 mm, gradient: 50% B to 85% B, 8 min, hold 2 min, flow rate 45 ml/min. LC-MS (Method A, retention time: 3.05 min), MS m/z 710 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173004B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-ee5bf2b4044f4110ae69103bea491c7f
Quellennotizuspto-grants-2007_02