HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-n-butylsulfonylamino-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Butanesulfonyl chloride | HCID 75430 | — |
| Reactant | 6-(2-amino-indan-5-yl)-4,5-dihydropyridazin-3(2H)-one | HCID 14071499 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-n-butylsulfonylamino-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane | HCID 18929785 | 74.9% |
Reaction Steps
6.3 g of n-butanesulfonyl chloride was added under ice cooling to 5.61 g of 2-amino-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane and 4.1 g of triethyl amine suspended in 50 ml of chloroform, and the mixture was stirred for 1 hour. Diluted hydrochloric acid was added to the reaction mixture, the chloroform layer was collected by separation, washed and dried, and then the solvent was removed. The resulting crystals were recrystallized from tetrahydrofuran-isopropyl ether to obtain 6.40 g of 2-n-butylsulfonylamino-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739132 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-0cdc02280fef4b28a3b27fc4c01a4933 |
| Source note | uspto-grants-1998_04 |