HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035868Generated: October 31, 2026
Ethanesulfonylchloride, 2-chloro- → HCID 66748760, compound
https://huagongshe.com/reaction/2035868
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66748374 | HCID 66748374 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66748760 | HCID 66748760 | — |
Reaction Steps
To a suspension of NaH (60%, 284 mg) in THF (dry) (25 mL) was added 2-chloroethanesulfonyl chloride (0.448 mL) at 0° C. and the mixture was stirred for 5 min at the same temperature. A solution of 3-(4-(2-methyl-4-(trifluoromethyl)phenoxy)phenyl)pyridin-2-amine (489 mg) in THF (dry) (40 mL) was added at 0° C. and the mixture was stirred at room temperature overnight. The mixture was quenched with water at 0° C. Water, EtOAc and THF were added and the extracted organic layer was washed with brine. Silica-gel was added to the organic layer and the volatiles were removed in vacuo. The mixture supported on silica-gel was purified by column chromatography (NH silica gel, eluted with MeOH in EtOAc) and washed with IPE to give the title compound (390 mg) as a white solid. A part of this was recrystallized from MeCN/IPE.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575154B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-650e8f14b4674611ba8e35b6dca2c1bc |
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| Source note | uspto-grants-2013_11 |
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