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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407494Erstellt: 24. Oktober 2026

Dichloromethane → HCID 23139542, Verbindung

https://huagongshe.com/de/reaction/407494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt4-Nitrophenyl chloroformateHCID 82129—
Edukt5-Amino-2,2-difluoro-1,3-benzodioxoleHCID 2736893—
EduktHCID 23139532HCID 23139532—
ProduktHCID 23139542HCID 2313954214%

Reaktionsschritte

To a solution of 4-(2-dimethylamino-ethoxy)-3-(2-methyl-2H-pyrazol-3-yl)-phenylamine (26.0 mg, 0.1 mmol) in methylene chloride (1 mL) pyridine (24.3 μL, 0.3 mmol) and 4-nitrophenyl chloroformate (20.2 mg, 0.1 mmol) were added and the mixture was stirred at room temperature for 1 hour. 5-Amino-2,2-difluoro-1,3-benzodioxole (11.6 μL, 0.1 mmol) was added, the reaction mixture stirred at room temperature for 48 hours and concentrated to give an oily residue that was subjected to a purification by flash chromatography (SiO2, CH2Cl2/MeOH gradient elution) to afford Compound 144 as an off-white solid in 14.0% yield. LCMS m/z (%)=460 (M+H, 100). 1H NMR (400 MHz, DMSO-d6) δ: 10.30 (s, 1H), 7.64 (d, J=8.96 Hz, 1H), 7.53 (s, 1H), 7.42 (s, 1H), 7.40-7.34 (m, 4H), 7.13 (d, J=8.92 Hz, 1H), 6.22 (s, 1H), 4.10 (t, J=5.56 Hz, 2H), 3.65 (s, 3H), 3.63 (s, 2H), 2.76-2.65 (m, 2H), 2.22 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754238B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-f0a0e4bf8a024e1694aa2b0095df4ecb
Quellennotizuspto-grants-2014_06