HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine Hydrochloride → Pyrimidine, 2,4-diamino-5-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18226-50-1 | HCID 3797843 | — |
| Reactant | HCID 15124901 | HCID 15124901 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Pyrimidine, 2,4-diamino-5-phenyl- | HCID 134761 | — |
Reaction Steps
This compound was prepared in a manner analogous to that of Example 2, Step E, using 4.9 grams (0.031 mole) of 1-cyano-1-phenyl-2-(N,N-dimethylamino)ethene, 11.8 grams (0.124 mole) of guanidine hydrochloride, and 21.4 grams (0.1 56 mole) of potassium carbonate in N,N-dimethylformamide. The yield of 2,4.-diamino-5-phenylpyrimidine was 0.7 gram; mp 162°-164° C. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05627189 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-2f07ad530ebd4cf2ab244702f5e57c7a |
| Source note | uspto-grants-1997_05 |