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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403601Generated: October 30, 2026

1-Methylpiperazine → HCID 70571655, compound

https://huagongshe.com/reaction/2403601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68106700HCID 68106700—
SolventDichloromethaneHCID 6344—
ProductHCID 70571655HCID 7057165595.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 4-nitrophenyl(3′-{[{[(tert-butoxycarbonyl)amino]acetyl}(methyl)amino]methyl}biphenyl-4-yl)carbamate (150 mg), DIPEA (36 mg), and dichloromethane (3 ml) was added 1-methylpiperazine (28 mg), followed by stirring at 50° C. for 5 hours. The reaction mixture was subjected to liquid separation with CHCl3-water, and the aqueous layer was extracted with CHCl3. The combined organic layer was dried over Na2SO4, and then the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (2% MeOH/CHCl3) to obtain tert-butyl (2-{methyl[(4′-{[(4-methylpiperazin-1-yl)carbonyl]amino}biphenyl-3-yl)methyl]amino}-2-oxoethyl)carbamate (132 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-2ad1b65bc1f7485fa2bf0790b9d826d9
Source noteuspto-grants-2014_08