HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409520Generated: October 30, 2026
Tert-Butanesulfinamide → HCID 86689260, compound
https://huagongshe.com/reaction/1409520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | 7-Bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-one | HCID 57475636 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 86689260 | HCID 86689260 | — |
Reaction Steps
A mixture of 7-bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-one (20 g, 64.4 mmol), 2-methyl-2-propanesulfinamide (23.42 g, 193 mmol) and titanium (IV) ethoxide (45.3 mL, 219 mmol) in dry THF 250 mL was heated at 75° C. overnight. The mixture was cooled to RT, then brine was added while stirring. The resulting suspension was filtered through celite, and the solid was washed with EtOAc. The filtrate was washed with brine, dried over sodium sulfate and concentrated. The crude material was purified by column chromatography with gradient of 0-30% EtOAc/Hexane to give the desired product as an orange solid. MS m/z=415.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921363B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-dc647cd6208e461e8933ff46b8d5dc64 |
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| Source note | uspto-grants-2014_12 |
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