HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butylamine → 4-Butylamino-6-chloro-2-methyl-5-nitronicotinic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Ethyl 4,6-dichloro-2-methyl-5-nitropyridine-3-carboxylate | HCID 12387594 | — |
| Reactant | 4-Butylamino-6-chloro-2-methyl-2-nitropyridine-3-carboxylic acid, ethyl ester | HCID 86734233 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Butylamino-6-chloro-2-methyl-5-nitronicotinic acid ethyl ester | HCID 12387598 | — |
Reaction Steps
139.5 g. of 4,6-dichloro-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester (0.5 Mol.) are dissolved in about 500 ml. of methanol. 60 g. of triethylamine are added and the solution is heated at reflux temperature. At this point, 36.5 g. of n-butylamine are added dropwise. The solvent is then removed in vacuo and 500 ml. of benzene are added to the residue. The triethylamine hydrochloride is filtered off and the solvent evaporated. The resulting oil is dissolved in 300 ml. of methanol and yields on cooling 110 g. of 4-butylamino-6-chloro-2-methyl-2-nitropyridine-3-carboxylic acid, ethyl ester (70%), m.p. 33°-35° (methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03996233 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-2c88c7993f9b4719be9f08060b9f5eec |
| Source note | uspto-grants-1976_12 |