HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598567Generated: October 25, 2026
Triethylamine → 2-n-butylsulfonylamino-5-[pyridazin-3(2H)-on-6-yl]indane
https://huagongshe.com/reaction/1598567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Butanesulfonyl chloride | HCID 75430 | — |
| Reactant | 2-amino-5-[pyridazin-3(2H)-on-6-yl]indane | HCID 18929773 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-n-butylsulfonylamino-5-[pyridazin-3(2H)-on-6-yl]indane | HCID 18929802 | 72.9% |
Reaction Steps
In 50 ml of dimethylformamide were dissolved 1.14 g of 2-amino-5-[pyridazin-3(2H)-on-6-yl]indane and 0.8 g of triethyl amine, and 1.25 g of n-butanesulfonyl chloride was added thereto. The mixture was stirred at 50° C for 30 minutes and then stirred at room temperature overnight. The solvent was removed, water was added to the residue, and crystals precipitated were collected by filtration. The resulting crystals were recrystallized from methanol to obtain 1.27 g of 2-n-butylsulfonylamino-5-[pyridazin-3(2H)-on-6-yl]indane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739132 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-5af222c59385436a96b3c24993006ea6 |
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| Source note | uspto-grants-1998_04 |
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