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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38117Erstellt: 24. Oktober 2026

Sodium hydride → Tert-butyl (trans)-2-(1,1'-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate

https://huagongshe.com/de/reaction/38117

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2-Chloro-1-(4-methylpiperazin-1-yl)ethanoneHCID 818173—
EduktTert-butyl(trans)-2-(1,1'-biphenyl-4-yl)cyclopropylcarbamateHCID 86658778—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl (trans)-2-(1,1'-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamateHCID 67448639—

Reaktionsschritte

To a suspension of 1.5 equiv of NaH in dry DMF (10 vols) at 0° C. was added a solution of tert-butyl(trans)-2-(1,1′-biphenyl-4-yl)cyclopropylcarbamate derivative (1 equiv) in dry DMF (2 vols) and stirr for 30 mins. Then, added a solution of 1-(chloroacetyl)-4-methylpiperazine (1.5 equiv) in dry DMF (10 mL) at 0° C., stirred for 1 h at 0° C. to RT. The progress of the reaction was monitored by TLC. After completion, reaction mixture was poured into ice water and extracted with EtOAC. The combined extracts were washed with water, brine, dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purifying by preparative HPLC to get tert-butyl (trans)-2-(1,1′-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate derivative

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524717B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c32a277b93bd4a4fa6a6d77eca32ddec
Quellennotizuspto-grants-2013_09