HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930052Generated: November 2, 2026
Potassium cyanate → HCID 136136827, compound
https://huagongshe.com/reaction/1930052
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 68562544 | HCID 68562544 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136136827 | HCID 136136827 | 8% |
Reaction Steps
To a solution of 2-amino-1-(2,4-difluorophenyl)-2-(3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone hydrochloride (1.18 g, 3.21 mmol) in DMF (10 mL) was added potassium cyanate (0.65 g, 8.0 mmol). The reaction mixture was stirred at about 110° C. for about 2 h. The temperature was reduced to about 80° C. and stirring continued for about 15 h. The solvent was removed under reduced pressure. The crude material was purified by RP-HPLC (Table 1, Method f). The appropriate fractions were combined and solvent removed under reduced pressure. The sample was dissolved in DCM (20 mL) and washed with saturated NaHCO3 solution (3×10 mL). The organic layer was dried over MgSO4, filtered, and solvent removed under reduced pressure to afford a solid that was dried under vacuum to give the title compound (0.09 g, 8%): LC/MS (Table 1, Method a) Rt=2.25 min; MS m/z: 357.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188083B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-76cca2134be64b48a5785b215db2531f |
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| Source note | uspto-grants-2012_05 |
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