HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239868Generated: November 1, 2026
N-(6-chloroimidazo[1,2-b]pyridazin-8-yl)benzenesulfonamide → HCID 178511643, compound
https://huagongshe.com/reaction/2239868
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(6-chloroimidazo[1,2-b]pyridazin-8-yl)benzenesulfonamide | HCID 86611749 | — |
| Reactant | HCID 178511674 | HCID 178511674 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178511643 | HCID 178511643 | — |
Reaction Steps
To N-(6-chloroimidazo[1,2-b]pyridazin-8-yl)benzenesulfonamide (100 mg, 0.325 mmol) from 1a was added trans-1,4-diaminocyclohexane (1000 mg, 8.77 mmol). The mixture was allowed to melt at 165° C. for 3 days. The melt was then cooled, water was added followed by extraction with dichloromethane. The organic layer was then concentrated in vacuo and purified by preparative HPLC. This gave 4.5 mg (2%) of the title compound as a TFA salt. 1H NMR (500 MHz, MeOH-D3) δ ppm 7.97 (2H, d, J=5 Hz), 7.85 (1H, s), 7.71 (1H, s), 7.63 (1H, m), 7.56 (2H, m), 6.63 (1H, s), 3.64 (1H, m), 3.12 (1H, m), 2.23-2.04 (4H, m), 1.51 (2H, m), 1.34 (2H, m). LC/MS m/e 387 (MH+). HPLC, 1.60 min. Waters Sunfire C18 4.6×50. 0%-100% B. B: 90% MeOH, 10% H2O, 0.1% TFA. A: 10% MeOH, 90% H2O, 0.1% TFA.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723336B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-1dee47a21e244e59bdc3fd6d90677f86 |
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| Source note | uspto-grants-2010_05 |
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