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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-1-(4-methylpiperazin-1-yl)ethanone | HCID 818173 | — |
| Reactant | tert-Butyl(trans)-2-[4-(benzyloxy)phenyl]cyclopropylcarbamate | HCID 15480693 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl (trans)-2-[4(benzyloxy)phenyl]cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524717B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-56d03ec35a2d4023a0d8ce3fad2c7d94 |
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| Source note | uspto-grants-2013_09 |
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