HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943423Generated: November 2, 2026
HCID 59624544, compound → HCID 178511619, compound
https://huagongshe.com/reaction/1943423
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59624544 | HCID 59624544 | — |
| Reactant | HCID 178511674 | HCID 178511674 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178511619 | HCID 178511619 | 71% |
Reaction Steps
A mixture of 8-(6-bromopyridin-2-ylamino)-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamide 17A (550 mg, 1.189 mmol) and trans-cyclohexane-1,4-diamine (1.086 g, 9.51 mmol) in NMP (4 mL) was heated at 100° C. overnight. The reaction mixture was cooled to room temperature, and then added to ice water. The yellow solid was collected by filtration, and rinsed with water. The still wet solid pad was azeotroped with DCM/MeOH three times. The resulting solid residue was treated with a small amount of MeOH, filtered and dried to give 17B (456 mg, 71%) as a yellow solid. MS (m+1)=540. HPLC Peak Rt=2.870 minutes. (Chromolith column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 minutes containing 0.1% TFA, 4 mL/min, monitoring at 220 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389527B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d79aab27551f44fdbbb97c04aace2555 |
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| Source note | uspto-grants-2013_03 |
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