HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butylamine → 4-Amino-6-butylamino-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 4-Amino-6-chloro-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester | HCID 54450212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Amino-6-butylamino-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester | HCID 54326304 | — |
Reaction Steps
26 g. of 4-amino-6-chloro-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester (0.1 mol.) in 300 ml. of alcohol and 15 g. of triethylamine are treated with 7.3 g. of butylamine for 30 minutes at reflux temperature. After this time, the solution is evaporated to dryness and 100 ml. of ethyl acetate are added to the residue. The triethylammonium chloride is filtered off, the solvent is evaporated and the remaining oil recrystallized from methanol. The yield of 4-amino-6-butylamino-2-methyl-5-nitropyridine-3-carboxylic acid ethyl ester is 25 g. (84%), m.p. 74°-76° (methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022779 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-dcade98641cc43ca924329af5d25183e |
| Source note | uspto-grants-1977_05 |