HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418314Generated: November 3, 2026
Hydrochloric Acid → HCID 131721181, compound
https://huagongshe.com/reaction/1418314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 131721162 | HCID 131721162 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131721181 | HCID 131721181 | 59.3% |
Reaction Steps
To a pyridine (5 mL) solution of 2-(5-amino-4-chloro-2-fluorophenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1, 3[2H, 7H]-dione (0.35 g, 1.2 mmol) was dropwise added p-toluenesulfonyl chloride (0.25 g, 1.3 mmol) under cooling in an ice-water bath, and the mixture was stirred for 2.5 hours at the ambient temperature. 1N Hydrochloric acid (60 mL) and ethyl acetate (40 mL) were added to the resulting mixture and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (20 mL×2 times), and the organic layer combined was washed with a saturated sodium chloride solution (100 mL) and dried over anhydrous magnesium sulfate. After removal of magnesium sulfate by filtration, the filtrate was evaporated to give crude product, which was purified by silica gel column (Wakogel C-200, ethyl acetate/hexane =1/2) to obtain a white solid of 2-[4-chloro-2-fluoro-5-(p-toluenesulfonylamino)phenyl]-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.32 g, yield:59.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05883049 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-745849f0c418483a868d74f9b376b28b |
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| Source note | uspto-grants-1999_03 |
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