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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38115Generated: October 27, 2026

Sodium hydride → Tert-butyl (trans)-2-[4(benzyloxy)phenyl]cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate

https://huagongshe.com/reaction/38115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-1-(4-methylpiperazin-1-yl)ethanoneHCID 818173—
Reactanttert-Butyl(trans)-2-[4-(benzyloxy)phenyl]cyclopropylcarbamateHCID 15480693—
SolventDimethylformamideHCID 6228—
ProductTert-butyl (trans)-2-[4(benzyloxy)phenyl]cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamateHCID 67369469—

Reaction Steps

To a suspension of 1.5 equiv of NaH in dry DMF (10 vols) at 0° C. was added a solution of ter-butyl(trans)-2-[4-(benzyloxy)phenyl]cyclopropylcarbamate (Intermediate C, 1 equiv) in dry DMF (2 vols) and stirr for 30 mins. Then, added was 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-[4(benzyloxy)phenyl]cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate derivative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524717B2
Source datasetuspto-grants-2013_09
ORD IDord-56d03ec35a2d4023a0d8ce3fad2c7d94
Source noteuspto-grants-2013_09