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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 513866Erstellt: 25. Oktober 2026

Hydrochloric Acid → HCID 178432276, Verbindung

https://huagongshe.com/reaction/513866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiphenylmethylidenehydrazineHCID 79304—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt7-fluoro-2-methyl-3H-benzimidazol-5-yl amineHCID 68005307—
Lösungsmittel4-MethylmorpholineHCID 7972—
ProduktHCID 178432276HCID 178432276—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

In a separate reaction container, 7-fluoro-2-methyl-3H-benzimidazol-5-yl amine (100 mg, 0.44 mmol), lithium bis(trimethylsilyl) amide (190 mg, 1.1 mmol), and benzophenone hydrazone (94.3 mg, 0.48 mmol) were dissolved in N-methyl-morpholine (0.5 ml) under a nitrogen atmosphere. Then, the prepared solution containing the catalyst was added thereto. After deaeration, this was heated and stirred at 100° C. under a nitrogen atmosphere for two hours. The reaction mixture was cooled to room temperature, and then an aqueous solution of 6 M hydrochloric acid (0.5 ml) was added thereto. The organic layer was isolated, and concentrated under reduced pressure. Thus, crude N-benzhydrylidene-N′-(7-fluoro-2-methyl-1H-benzimidazol-5-yl)-hydrazine was obtained. The obtained crude product was used in subsequent reactions without being purified.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09102692B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-153fc8c3594f4a33b3ecfdba3608cf17
Quellennotizuspto-grants-2015_08