HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyrimidine → 2-Aminopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyrimidine | HCID 7978 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Product | 2-Aminopyridine | HCID 10439 | — |
| Product | 2-Amino-5-nitropyridine | HCID 77888 | — |
Reaction Steps
Alternatively, 2-chloro-5-nitropyridine can be prepared using the procedure described in the Journal Chemical Society 9 (1941), starting with 2-aminopyrimidine. Nitration of 2-aminopyridine gives 2-amino-5-nitropyridine, which can be converted into 2-hydroxy-5-nitropyridine by a diazonium reaction. Subsequent heating of 2-hydroxy-5-nitropyridine in a phosphorous pentachloride/phosphorous oxychloride mixture yields 2-chloro-5-nitropyridine. The synthesis is summarized below: ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04371736 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-25585783180a44ba800a7b6bf00276d2 |
| Source note | uspto-grants-1983_02 |