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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(6-chloroimidazo[1,2-b]pyridazin-8-yl)benzenesulfonamideHCID 86611749—
ReactantHCID 178511674HCID 178511674—
SolventWaterHCID 962—
ProductHCID 178511643HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-1dee47a21e244e59bdc3fd6d90677f86
Source noteuspto-grants-2010_05