HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Butylpyridin-2-amine → HCID 178476211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Butylpyridin-2-amine | HCID 18428650 | — |
| Reactant | 2-Imino-4-methylpiperidine acetate | HCID 178475870 | — |
| Product | HCID 178476211 | HCID 178476211 | — |
Reaction Steps
The method of preparation of 2-imino-4-methylpiperidine acetate was used to convert 2-amino-5-(n-butyl)pyridine to the title compound except platinum oxide was used as the catalyst. Product was triturated with ether to give a white solid. The analysis of the product was found to be consistent with the proposed structure. MH+=155; 1H NMR (D2O): δ3.35-3.25 (m, 1H); 2.85-2.75 (m, 1H); 2.60-2.35 (m, 2H); 1.85-1.55 (m, 2H); 1.75 (s, 3H); 1.35-1.05 (m, 7H); 0.75-0.65 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046211 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-25bed92e1e894a0c923897d452f688e8 |
| Source note | uspto-grants-2000_04 |