Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | 2-aminomethyl-5-[pyridazin-3(2H)-on-6-yl]indane hydrobromide | HCID 21476291 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21476295 | HCID 21476295 | 82.5% |
Reaction Steps
In a mixed solution of 30 ml of ethyl acetate and 30 ml of tetrahydrofuran was suspended 3.22 g of 2-aminomethyl-5-[pyridazin-3(2H)-on-6-yl]indane hydrobromide. A sodium carbonate aqueous solution (5.30 g/30 ml of water) was added to the suspension. Under ice cooling, 3.32 g of ethanesulfonyl chloride dissolved in 10 ml of tetrahydrofuran was added to the mixture, and the resulting mixture was stirred for 3 hours. 300 ml of ethyl acetate was added to the mixture. After the organic layer was collected by separation, washed with water and dried, and the solvent was removed. The residue was purified by silica gel column chromatography (chloroform-methanol (100:3)) to obtain 2.75 g of 2-(ethylsulfonylaminomethyl)-5-[pyridazin-3(2H)-on-6-yl]indane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686452 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-3c61e454e9b64a54b7055d90cbe2b4f2 |
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| Source note | uspto-grants-1997_11 |
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