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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2382003Erstellt: 25. Oktober 2026

Sodium bis(trimethylsilyl)amide → 2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (5-methanesulfonyl-indol-1-yl)-amide

https://huagongshe.com/reaction/2382003

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt5-Methanesulfonyl-indol-1-ylamineHCID 68555592—
Edukt2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid chlorideHCID 87495795—
LösungsmittelPyridineHCID 1049—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (5-methanesulfonyl-indol-1-yl)-amideHCID 5920005716,4%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

2.0 M of NaHMDS (sodium bis(trimethylsilyl)amide) in THF is added to a stirred solution of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid chloride (0.72 mmol) and 5-methanesulfonyl-indol-1-ylamine (0.72 mmol) and in anhydrous pyridine (10 mL) at rt. The reaction mixture is stirred at 90° C. overnight and then concentrated in vacuo. The residue is purified ny silica gel chromatography eluting with 1.5% MeOH in DCM to afford 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (5-methanesulfonyl-indol-1-yl)-amide (50 mg, 8%) as a solid. MS: 425 (M+H); 1H NMR (300 MHz, CDCl3): δ 2.86 (s, 3H), 3.02 (s, 3H), 6.55 (s, H) 6.92 (d, H), 7.17-7.38 (m, 3H), 7.53 (m, H), 7.78 (s, H), 8.27 (d, H), 8.38 (d, H), 9.16 (s, H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08258130B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-c165caed26644a2e90b476843f8ef8dc
Quellennotizuspto-grants-2012_09