HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060025Generated: October 31, 2026
Cyanamide → N-cyano-4-(4-methoxypyridin-2-yl)-2-nitroaniline
https://huagongshe.com/reaction/1060025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzene | HCID 18667563 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-cyano-4-(4-methoxypyridin-2-yl)-2-nitroaniline | HCID 18667498 | 89.4% |
Reaction Steps
To a solution of cyanamide (101 mg) in N,N-dimethylformamide (15 ml) was added sodium hydride (60% dispersion in mineral oil, 90 mg), and the resultant suspension was stirred at ambient temperature for 30 minutes. To the suspension was added 1-chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzene (264 mg), and the mixture was stirred at 80° C. for 4 hours. The mixture was poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate three times. The combined organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was triturated with diisopropyl ether, filtered and dried under reduced pressure to give N-cyano-4-(4-methoxypyridin-2-yl)-2-nitroaniline (241 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521643B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-9ddb66a6987e4c3a98f13b59cef3053b |
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| Source note | uspto-grants-2003_02 |
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