HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419174Generated: October 30, 2026
Methanesulfonyl chloride → HCID 57942459, compound
https://huagongshe.com/reaction/419174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 57942452 | HCID 57942452 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57942459 | HCID 57942459 | — |
Reaction Steps
To a solution of N-[2-(2-amino-pyridine-4-carbonyl)-5-chloro-pyridin-3-yl]-N-methoxymethyl-4-methyl-3-trifluoromethyl-benzenesulfonamide (140 mg, 0.272 mmol) in pyridine (0.75 mL) was added methanesulfonyl chloride (0.042 mL, 0.544 mmol). The reaction was warmed to 50° C. and stirred 2.5 h. The resultant mixture was quenched with 10% HCl, diluted with EtOAc, and the organic layer washed with 10% HCl and saturated sodium bicarbonate. The combined organics were dried with sodium sulfate, concentrated in vacuo, and purified via automated silica gel chromatography to produce the desired sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093247B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-f638bd7807534aa393dc61df4e892b75 |
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| Source note | uspto-grants-2012_01 |
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