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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407372Erstellt: 24. Oktober 2026

1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene → 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(4-Chloro-3-trifluoromethyl-phenyl)-urea

https://huagongshe.com/de/reaction/407372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-4-isocyanato-2-(trifluoromethyl) benzeneHCID 2733265—
Edukt3-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-methoxyanilineHCID 11572741—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(4-Chloro-3-trifluoromethyl-phenyl)-ureaHCID 1151901183,3%

Reaktionsschritte

3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenylamine (0.035 g, 0.12 mmol) was treated with 4-chloro-3-(trifluoromethyl)phenyl isocyanate (0.027 g, 0.12 mmol, 1.0 equiv.) in CH2Cl2 (2 mL), in a similar manner as described in Example 1.2 to afford Compound 6 (0.051 g, 0.10 mmol, 81%) as a white solid. LCMS m/z (%)=503 (M+H79Br35Cl, 78), 505 (M+H81Br35Cl, 100), 507 (M+H81Br37Cl, 28). 1H NMR (400 MHz, acetone-d6) δ: 8.52 (s, 1H), 8.27 (s, 1H), 8.13 (s, 1H), 7.74 (b, J=8.7 Hz, 1H), 7.68 (d, J=9.0 Hz, 1H), 7.53 (d, J=8.7 Hz, 1H), 7.49 (s, 1H), 7.43 (s, 1H), 7.14 (d, J=9.0 Hz, 1H), 3.82 (s, 3H), 3.68 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754238B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-445cba3de6554bd19b0eedc302c5af43
Quellennotizuspto-grants-2014_06