HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Methyl-2-nitropyridin-3-ol → HCID 178475862, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Methyl-2-nitropyridin-3-ol | HCID 84801 | — |
| Reactant | 2-Imino-4-methylpiperidine acetate | HCID 178475870 | — |
| Product | HCID 178475862 | HCID 178475862 | — |
Reaction Steps
The method of preparation of 2-imino-4-methylpiperidine acetate was used to convert 3-hydroxy-6-methyl-2-nitropyridine to the title compound except the reaction was run at 55° C. Product was obtained as a dark solid which was recrystallized from EtOH/EtOAc to give light amber crystals. The analysis of the product was found to be consistent with the proposed structure. m.p. 158-160° C. MH+=129; 1H NMR (D2O): δ4.40-4.30 (m, 1H); 3.60-3.40 (m, 1H); 2.00-1.40 (m, 4H); 1.72 (s, 3H); 1.10 (d, J=7 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046211 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-c755f41b48f84d03b8c3bb87b517cb6e |
| Source note | uspto-grants-2000_04 |