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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 61597Erstellt: 24. Oktober 2026

Diisopropylethylamine → 2-(3-(4-(1h-Indazol-5-ylamino)quinazolin-2-yl)phenoxy)-n-(cyanomethyl)acetamide

https://huagongshe.com/de/reaction/61597

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktAminoacetonitrile sulfate (1:1)HCID 196971—
EduktPyBOPHCID 2724699—
Edukt2-(3-(4-((1H-indazol-5-yl)amino)quinazolin-2-yl)phenoxy)acetic acidHCID 59361988—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(3-(4-(1h-Indazol-5-ylamino)quinazolin-2-yl)phenoxy)-n-(cyanomethyl)acetamideHCID 11950521—

Reaktionsschritte

A suspension of 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)acetic acid (70 mg, 0.14 mmol), PyBOP® (40 mg, 0.077 mmol), DIEA (24 μL, 0.14 mmol) in dry CH2Cl2:DMF (2:0.1 mL) was stirred at RT for 15 minutes. To this solution of activated acid was added aminoacetonitrile monosulfate (14 mg, 0.091 mmol). After 30 minutes, 1.0 equivalent of DIEA and 0.55 equivalents of PyBOP® were added. After stirring the solution for 15 minutes, 0.65 equivalents of aminoacetonitrile monosulfate were added and the mixture was stirred for an additional 30 minutes. The solvent was removed in vacuo and the crude product was purified using prep HPLC (15-40_90 mins) to afford 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(cyanomethyl)acetamide. (12 mg, 0.027 mmol, 19%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440961B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-f89e62fea6d8459780d59e2aaa880108
Quellennotizuspto-grants-2016_09