HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333560Generated: October 30, 2026
Methylamine → N-Methyl-3-nitro-2-pyridinamine
https://huagongshe.com/reaction/333560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| Product | N-Methyl-3-nitro-2-pyridinamine | HCID 556349 | 98.5% |
Reaction Steps
Methylamine (33% in EtOH) (110 mL, 883 mmol) was placed in a 500 mL three necked round bottom flask. It was cooled to 0° C. using ice bath. 2-chloro-3-nitropyridine (20 g, 126 mmol) was added to the above solution in portions as this is an exothermic reaction. After the addition was complete the reaction mixture was stirred for 2 h at 0° C. and later 1 h at room temperature. Solvent was concentrated and residue was taken in 500 mL of water and extracted with EtOAc 3×150 mL. Combine organic layer was dried over Na2SO4, filtered and concentrated to give a bright orangish yellow solid (19 g, 98.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883322B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-8b6e3727169845798390ba13f3e9556e |
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| Source note | uspto-grants-2014_11 |
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