HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268039Generated: October 29, 2026
Methanesulfonyl chloride → HCID 12019007, compound
https://huagongshe.com/reaction/1268039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 15907988 | HCID 15907988 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 12019007 | HCID 12019007 | — |
Reaction Steps
To an ice cooled solution of N-(4-{3-[3,5-dichloro-4-(2-hydroxy-ethoxy)-phenyl]-thioureido}-phenyl)-acetamide (0.20 g) in pyridine (2 mL) and tetrahydrofuran (0.5 mL) is added methanesulfonyl chloride (0.11 g) and the solution is stirred at 0° C. for 45 minutes. The reaction mixture is then diluted with ethyl acetate, washed successively twice with 2% aqueous hydrochloric acid, once with saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. After removing the solvents by evaporation under reduced pressure the resulting residue is recrystallized from acetone-hexanes to give the desired product as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06555561B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-ed7aaf20bde94a2291429856044321c0 |
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| Source note | uspto-grants-2003_04 |
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