HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403601Generated: October 30, 2026
1-Methylpiperazine → HCID 70571655, compound
https://huagongshe.com/reaction/2403601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68106700 | HCID 68106700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70571655 | HCID 70571655 | 95.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802679B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-2ad1b65bc1f7485fa2bf0790b9d826d9 |
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| Source note | uspto-grants-2014_08 |
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