HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-Methyl-5-nitro-6-(4,5,7,8-tetrahydro-thieno[2,3-d]azepin-6-yl)-3H-pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4H,5H,6H,7H,8H-thieno[2,3-d]azepine | HCID 11513777 | — |
| 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-thieno[2,3-d]azepin-6-yl)-3H-pyrimidin-4-one | HCID 135671162 | — |
Reaction Steps
According to the method described in example 1c 6-bromo-2-methyl-5-nitro-3H-pyrimidin-4-one (example 1a) was treated with 5,6,7,8-tetrahydro-4H-thieno-[2,3-d]azepine [J. Heterocycl. Chem. (1985), 22(4), 1011-16] in N,N-dimethylformamide in the presence of N-ethyl-di-isopropylamine at room temperature to yield the title compound as yellow solid; m.p.>200° C.; MS: [M−H]−=305.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06369222B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-7116dad7195843bdba0712cdd1e555ff |
| Source note | uspto-grants-2002_04 |