HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-methyl-5-nitro-6-(4,5,7,8-tetrahydro-thiazolo[4,5-d]azepin-6-yl)-3H-pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5,6,7,8-tetrahydro-4H-thiazolo[4,5-d]azepine | HCID 22620747 | — |
| Reactant | 6-bromo-2-methyl-5-nitro-3H-pyrimidin-4-one | HCID 135617193 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-methyl-5-nitro-6-(4,5,7,8-tetrahydro-thiazolo[4,5-d]azepin-6-yl)-3H-pyrimidin-4-one | HCID 135671155 | — |
Reaction Steps
In analogy to the procedure described in example 1c 6-bromo-2-methyl-5-nitro-3H-pyrimidin-4-one (example 1a) was treated with the 5,6,7,8-tetrahydro-4H-thiazolo[4,5-d]azepine in N,N-dimethylformamide in the presence of potassium carbonate at room temperature to yield the 2-methyl-5-nitro-6-(4,5,7,8-tetrahydro-thiazolo[4,5-d]azepine-6-yl)-3H-pyrimidin-4-one as yellow amorphous solid; MS: (M−H]−=306.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06369222B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-66daebd3d24c4bcb8121f99ebe93eb38 |
| Source note | uspto-grants-2002_04 |