HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73244Generated: October 29, 2026
Methanesulfonyl chloride → HCID 178441166, compound
https://huagongshe.com/reaction/73244
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59703946 | HCID 59703946 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178441166 | HCID 178441166 | 79.7% |
Reaction Steps
To a solution of 172 mg (0.52 mmol) of N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-2-(pyrrolidin-3-ylmethylsulfanyl)-propionamide (prepared according to Method I, step 1) and 0.18 mL (1.04 mmol) of N,N-diisopropylethylamine in THF were added 0.16 mL (2.11 mmol) of methanesulfonyl chloride. The reaction was heated within a microwave to 90° C. for 0.5 h. The mixture was concentrated under reduced pressure. The residue was dissolved in DCM (5 mL) and washed with saturated aqueous NaHCO3 solution (5 mL). The organic layer was dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure to afford 168 mg of N-(5-tert-butyl-isoxazol-3-yl)-2-(1-methanesulfonyl-pyrrolidin-3-ylmethylsulfanyl)-2-methyl-propionamide, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829034B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2a2529c63b77412a91e1cd95f8ee4bd0 |
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| Source note | uspto-grants-2014_09 |
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