HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium → HCID 178418410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178418346 | HCID 178418346 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178418410 | HCID 178418410 | — |
Reaction Steps
The final product, 4-chloro-N-(imidazolin-2-ylidene)-6-methoxy-2-methyl-5-pyrimidinamine is synthesized by first preparing sodium methoxide in situ from anhydrous methanol and sodium. The fifth intermediate, N-(1-acetylimidazolin-2-ylidene)-4,6-dichloro-2-methyl-5-pyrimidinamine, is added and the reaction mixture brought to a boil. From 15 minutes to 1 hour after the reaction mixture is brought to a boil, further sodium methoxide is added and the reaction mixture is maintained at a boil for from 15 minutes to 1 hour to afford 4-chloro-N-(imidazolin-2-ylidene)-6-methoxy-2-methyl-5-pyrimidinamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05732717 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-034dc9437bee48c3847af5a6f9237cbd |
| Source note | uspto-grants-1998_03 |