HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772778Generated: November 3, 2026
Methanesulfonyl chloride → HCID 86651906, compound
https://huagongshe.com/reaction/1772778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67054912 | HCID 67054912 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86651906 | HCID 86651906 | 102.1% |
Reaction Steps
To a mixture of benzyl 4-(2-hydroxypropyl)piperazine-1-carboxylate (from step 1, 1.7 g, 6.1 mmol) in DCM (20 mL) was added DIPEA (2.1 mL, 12 mmol) followed by methanesulfonyl chloride (0.70 mL, 9.0 mmol) at 0° C. The reaction was stirred at 0° C. for 2 h. The reaction was quenched with saturated NaHCO3 solution and extracted with DCM. The combined organic layers were washed with brine, dried over MgSO4 and concentrated to provide crude product (2.22 g) which was used in next step without further purification. LCMS calculated for C16H25N2O5S(M+H)+: m/z=357.1; Found: 357.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249145B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-ae22d9873b964d94b8a1f980554dabc4 |
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| Source note | uspto-grants-2016_02 |
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