HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622671Generated: October 30, 2026
Ethanesulfonylchloride, 2-chloro- → HCID 66748125, compound
https://huagongshe.com/reaction/1622671
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66748421 | HCID 66748421 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66748125 | HCID 66748125 | — |
Reaction Steps
To a suspension of NaH (60%, 136 mg) in THF (dry) (10 mL) was added 2-chloroethanesulfonyl chloride (0.214 mL) at 0° C. and the mixture was stirred for 5 min at the same temperature. A solution of 3-{4-[(3-fluorobenzyl)oxy]phenyl}pyridin-2-amine (200 mg) in THF (dry) (10 mL) was added at 0° C. and the mixture was stirred at room temperature under nitrogen overnight. The mixture was quenched with water at 0° C. carefully. Water was added to form precipitates which were washed with water, hexane and collected. The precipitate was sonicated in EtOAc and the insoluble material was collected to give 9-{4-[(3-fluorobenzyl)oxy]phenyl}-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide (317.7 mg) as an off-white solid. This was crystallized from MeOH-THF/IPE to give an off-white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778934B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-19afb20b222249bd959c9df4f99081dd |
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| Source note | uspto-grants-2014_07 |
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