HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291566Generated: November 1, 2026
Methanesulfonyl chloride → HCID 21278904, compound
https://huagongshe.com/reaction/2291566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-[4-(4-Amino-3-methylphenyl)piperazin-1-yl]ethan-1-one | HCID 21278912 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21278904 | HCID 21278904 | — |
Reaction Steps
1-Acetyl-4-(4-amino-3-methylphenyl)piperazine (7.89 g) was dissolved in pyridine (130 ml). Methanesulphonyl chloride (7.9 ml) was added dropwise with stirring. The mixture was reduced in volume after 2 hours by evaporation and then stirred overnight. The resulting slurry was partitioned between water (125 ml) and dichloromethane (100 ml), and the aqueous layer was further extracted with dichloromethane (2×100 ml), 5% methanol in dichloromethane (2×100 ml), and ethyl acetate (2×125 ml). The combined organic layers were dried (sodium sulphate) and evaporated, and the residue was chromatographed in 5% methanol in dichloromethane over t.l.c. grade silica, the product-containing fractions, after evaporation, yielding a foam (5.93 g), Rf 0.29 (5% methanol/dichloromethane/silica), used directly in step (D). A small sample from a second run was recrystallized from ethyl acetate/hexane, m.p. 153°-4°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04797401 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-733c95189d184b8bb461a72b04062d3e |
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| Source note | uspto-grants-1989_01 |
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