HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972614Generated: November 2, 2026
Aniline → N-(((2S)-1,4-dibenzyl-2-piperazinyl)methyl)aniline
https://huagongshe.com/reaction/1972614
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate | HCID 86670397 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(((2S)-1,4-dibenzyl-2-piperazinyl)methyl)aniline | HCID 66584230 | 73.2% |
Reaction Steps
A 20-mL vial was charged ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate (1.01 g, 2.70 mmol, Example 184, Step 1), aniline (1.30 mL, 14.3 mmol, Alfa Aesar, Ward Hill, Mass.) and MeOH (12 mL). The reaction mixture was sealed and heated at 140° C. for 30 min in an Initiator microwave reactor (Biotage AB, Inc., Uppsala, Sweden). The mixture was allowed to cool to room temperature and then concentrated in vacuo. The crude product was purified by column chromatography (50 g of silica gel, (2 M NH3 in MeOH) in CH2Cl2 0 to 5%) to afford N-(((2S)-1,4-dibenzyl-2-piperazinyl)methyl)aniline (0.734 g) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431563B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-7c5d0a86eba341358c58c8bc608791cc |
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| Source note | uspto-grants-2013_04 |
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