HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393441Generated: October 30, 2026
Dimethylformamide dimethyl acetal → N,N-Dimethyl-2-(2-acetylamino-5-nitropyridin-4-yl)ethenamine
https://huagongshe.com/reaction/2393441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | N-(4-methyl-5-nitropyridin-2-yl)acetamide | HCID 13567013 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-Dimethyl-2-(2-acetylamino-5-nitropyridin-4-yl)ethenamine | HCID 53811652 | 76.2% |
Reaction Steps
To a solution of 2-acetylamino-4-methyl-5-nitropyridine (33.8 g, 0.173 mol) in dry DMF (300 mL) was added dimethylformamide dimethyl acetal (50.7 mL, 0.381 mol) and the mixture heated at 90° C. for 90 min. The solvent was evaporated in vacuo using toluene as an azeotrope. The residue was triturated with ether and the solid collected by filtration to give the title compound (33 g, 76%) as an orange solid. mp 193°-196° C. 1H NMR (250 MHz, CDCl3) δ 2.23 (3H, s), 3.04 (6H, s), 6.12 (1H, d, J=13.1Hz), 7.43 (1H, d, J=13.1Hz), 8.17 (1H, br s), 8.27 (1H, s) and 8.83 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807857 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-9dbf4cbab6ee4efca335239cf1642829 |
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| Source note | uspto-grants-1998_09 |
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