HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972559Generated: November 2, 2026
Methanesulfonyl chloride → ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate
https://huagongshe.com/reaction/1972559
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | [(2R)-1,4-dibenzylpiperazin-2-yl]methanol | HCID 9994741 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate | HCID 86670397 | 87.5% |
Reaction Steps
A mixture of (R)-(1,4-dibenzylpiperazin-2-yl)methanol (4.00 g, 13.49 mmol, US2007/0088039) and Hünig's base (2.35 mL, 13.49 mmol) in CH2Cl2 (27 mL) was stirred at 0° C. and methanesulfonyl chloride (1.04 mL, 13.49 mmol) was added drop-wise. The reaction mixture was filtered through a short pad of silica gel, using 19:1 CH2Cl2/Et2O (1000 mL) to rinse. The filtrate was concentrated in vacuo while maintaining the temperature below 25° C. Diethyl ether was added to the residue, the resulting slurry was placed in a sonicator for 1 min, filtered through a fitted funnel and the filtrate was concentrated to give a white solid ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate (4.42 g).
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-c712bca14f8a45769e83740a3d07432c |
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| Source note | uspto-grants-2013_04 |
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