HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyrimidine → 2-amino-5-bromo-N-pyrimidin-4-yl-pyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyrimidine | HCID 68958 | — |
| Reactant | 2-Amino-5-bromonicotinic acid | HCID 737445 | — |
| Reactant | HCID 71061295 | HCID 71061295 | — |
| Product | 2-amino-5-bromo-N-pyrimidin-4-yl-pyridine-3-carboxamide | HCID 71061157 | — |
Reaction Steps
6.1 Reaction of 2-amino-5-bromo-pyridine-3-carboxylic acid with pyrimidin-4-amine according to the synthesis described for “A1” step 1, gives 2-amino-5-bromo-N-pyrimidin-4-yl-pyridine-3-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273029B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e32e5e2c0a884bbb9bc25842561e1ee1 |
| Source note | uspto-grants-2016_03 |