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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291566Generated: November 1, 2026

Methanesulfonyl chloride → HCID 21278904, compound

https://huagongshe.com/reaction/2291566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-[4-(4-Amino-3-methylphenyl)piperazin-1-yl]ethan-1-oneHCID 21278912—
SolventPyridineHCID 1049—
ProductHCID 21278904HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797401
Source datasetuspto-grants-1989_01
ORD IDord-733c95189d184b8bb461a72b04062d3e
Source noteuspto-grants-1989_01