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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 646656Erstellt: 25. Oktober 2026

Hexamethyldisilazane → Letrozole

https://huagongshe.com/reaction/646656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexamethyldisilazaneHCID 13838—
Edukt4-FluorobenzonitrileHCID 14517—
EduktSodium amideHCID 24533—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
EduktHCID 178509721HCID 178509721—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelDimethylacetamideHCID 31374—
ProduktLetrozoleHCID 3902—
Produkt4-FluorobenzonitrileHCID 14517—
ProduktHCID 178509721HCID 178509721—

Reaktionsschritte

Most preferably, the base is sodium bis(trimethylsilyl)amide, which may be prepared from hexamethyldisilazane and sodium amide, or purchased as a 40 percent solution in tetrahydrofuran. To avoid reaction between the 4-fluorobenzonitrile V and the sodium bis(trimethylsilyl)amide, the base is preferably added gradually to the mixture of synthons (all known procedures first generate the anion of intermediate III prior to bringing it into contact with 4-fluorobenzonitrile V). Approximately equimolar amounts of the intermediate III and 4-fluorobenzonitrile V in dimethylacetamide, dimethylformamide, or tetrahydrofuran provide a yield of about 85 percent by weight of pure letrozole after isolation and purification. As no stoichiometric excess of 4-fluorobenzonitrile V is required, any side-reactions with the base are believed to be negligible.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07705159B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-af800d977dea40cdaf93e3d2be94c129
Quellennotizuspto-grants-2010_04