HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491613Generated: October 26, 2026
1,2-Dichloroethane → HCID 178485501, compound
https://huagongshe.com/reaction/491613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Chloro-4-isothiocyanato-2-(trifluoromethyl)benzene | HCID 520026 | — |
| Reactant | 4-(3,4-Diamino-phenoxy)-pyridine-2-carboxylic acid methylamide | HCID 17756492 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178485501 | HCID 178485501 | — |
Reaction Steps
To a solution of 4-(3,4-diamino-phenoxy)-pyridine-2-carboxylic acid methylamide (Step B) (0.07 g, 0.27 mmol) in 20 mL CH3CN was added dropwise, over 5 min, a solution 1-chloro-4-isothiocyanato-2-trifluoromethyl-benzene (0.055 g, 0.27 mmol) in 10 mL CH3CN. The reaction was stirred 18 h at RT. The reaction was diluted with 10 mL CH3CN, then EDC (0.078 g, 0.41 mmol) was added. The reaction was heated at 80° C. for 3 h. The reaction was cooled to RT and concentrated in vacuo. The crude mix was dissolved in EtOAc and water. The layers were separated, and the organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography using a hexane-EtOAc gradient to yield the title compound. MS (MH+)=461.9; MW Calc'd 461.09 for C21H15ClF3N5O2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531553B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-390f6d182b5b4dfeb747962d784f5010 |
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| Source note | uspto-grants-2009_05 |
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