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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 631528Erstellt: 25. Oktober 2026

Diisopropylethylamine → HCID 44242929, Verbindung

https://huagongshe.com/reaction/631528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Eduktphenyl 3-tert-butyl-1-methyl-1H-pyrazol-5-ylcarbamateHCID 46196890—
Edukt3-(6-Methoxy-7-(2-methoxyethoxy)quinazolin-4-yloxy)anilineHCID 66875805—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
ProduktHCID 44242929HCID 44242929—

Reaktionsschritte

The procedure in 138B was used to react the carbamate from Example 157A (123 mg, 0.45 mmol) with 3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-yloxy)aniline from Example 117B (103 mg, 0.30 mmol). To this solution was added diisopropylethyl amine (78 μL, 0.45 mmol) and DMAP (3.6 mg, 0.03 mmol). The reaction was concentrated to dryness. The resulting oil purified by silica gel chromatography eluting with ethyl acetate/dichloromethane 10-50% over 60 minutes. The main peak concentrated to a solid weighing 126 mg. 1H (DMSO-d6) 9.10 (s, 1H), 8.70 (s, 2H), 7.65 (m, 2H), 7.50 (m, 2H), 7.30 (m, 1H), 7.15 (s, 1H), 6.95 (m, 1H), 6.00 (s, 1H), 4.40 (s, 2H), 4.00 (s, 3H), 3.85 (s, 2H), 3.60 (s, 3H), 3.40 (s, 3H), 1.25 (s, 9H). LCMS (ESI) m/z 521 (M+H)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09320739B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-8f423ec6736e468d9748912585177e1f
Quellennotizuspto-grants-2016_04