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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 652135Erstellt: 23. Oktober 2026

Sodium hydride → 1-Cyclopropylmethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide

https://huagongshe.com/de/reaction/652135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt(Chloromethyl)cyclopropaneHCID 80013—
EduktEther hydrobromideHCID 86739792—
EduktHCID 178480237HCID 178480237—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Cyclopropylmethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromideHCID 1403250932%

Reaktionsschritte

To a stirred mixture of 1.19 g of sodium hydride (50% oil dispersion) in 65 ml of dimethylformamide was added, dropwise, 4.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 20 ml of hot dimethylformamide. The mixture was stirred for 1 hr at ambient temperature and then 1.40 g of chloromethylcyclopropane in 10 ml of dimethylformamide was added dropwise. The reaction mixture was stirred for 21/2 days at ambient temperature. The reaction mixture was quenched with water, extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and saturated hydrogen bromide/ether solution was added dropwise to precipitate a salt. The salt was recrystallized from toluene and ethyl acetate to yield 2.8 g (32%) of product, mp 177°-179° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04670447
Quelldatensatzuspto-grants-1987_06
ORD IDord-e0f9a700d0ef43138969234d00ec0ad2
Quellennotizuspto-grants-1987_06