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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 737002Erstellt: 24. Oktober 2026

Triethylamine → 4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamide

https://huagongshe.com/de/reaction/737002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-Chloro-1H-indazoleHCID 95894—
EduktHCID 58975125HCID 58975125—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamideHCID 5897515283%

Reaktionsschritte

Dissolve 3-chloro-1H-indazole (120 mg, 0.79 mmol) and 4-(4-fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (114 mg, 0.35 mmol) in CH2Cl2 (2.0 mL) and treat with Et3N (50 L, 0.36 mmol). Stir the solution for 1 h at RT, then dilute with additional CH2Cl2 (20.0 mL) and wash with satd aq. NaHCO3 (15 mL). Dry, filter, and concentrate the organic phase and purify the crude material by flash chromatography (100% hexanes to 50% EtOAc/hexanes linear gradient) to give the title compound (129 mg, 83%) as a white foam. MS (ES+) 443.9 (M+1)+, (ES−) 442.0 (M−1)−. 1H NMR (400 MHz, CDCl3): δ 8.17 (d, 1H, J=8.3), 8.03 (d, 2H, J=8.2), 7.83 (d, 2H, J=8.9), 7.64 (m, 2H), 7.41 (t, 1H, J=7.4), 7.27 (m, 2H), 7.01 (t, 2H, J=8.9), 6.31 (br s, 1H), 4.57 (d, 2H, J=5.9).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595339B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-7d1af9b7d86a421cbcdeaaa5266986a4
Quellennotizuspto-grants-2009_09