HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloropyrazine → HCID 178479476, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloropyrazine | HCID 73277 | — |
| Reactant | 2-Methyl-2-thiopseudourea sulfate | HCID 75270 | — |
| Reactant | 3,5-Diamino-N-(2-aminoethyl)-6-chloropyrazine-2-carboxamide | HCID 15148129 | — |
| Reactant | HCID 178513210 | HCID 178513210 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178479476 | HCID 178479476 | — |
Reaction Steps
Dissolve the product of Step 1 (100 mg) and 2-methyl-2-thiopseudourea sulfate (122 mg) in water (0.5 ml) and MeOH (0.5 ml) and heat on a steam bath for 1 hour. If all the starting chloropyrazine is not reacted, add more pseudourea and repeat the procedure. Triturate the resulting residue in EtOH to obtain the sulfate salt of the title compound. Chromatograph the product on a high pressure reversed phase prep C18 column (Dynamax), eluting with MeOH:H2O (40:60), 0.2% TFA, at 10 ml/min., followed by a C18 Magnum 20 column (Whatman), eluting with MeOH:H2O (30:70), 0.2% TFA. Dissolve the resultant residue in 1N HCl, evaporate the solvent, redissolve in water and lyophilize to obtain the title compound as a yellow solid, m.p. 100° (d), M+ =272.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04803206 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-92d9c5d2a3cd4eca91a7dff6f9962d82 |
| Source note | uspto-grants-1989_02 |