HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylpiperidine → HCID 135617199, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-bromo-2-methyl-5-nitro-3H-pyrimidin-4-one | HCID 135617193 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135617199 | HCID 135617199 | — |
Reaction Steps
In analogy to the procedure described in example 1, the 6-bromo-2-methyl-5-nitro-3H-pyrimidin-4-one (as prepared in Eur. Pat. Appl. EP 1074549 A2) was treated with the 4-phenylpiperidine in N,N-dimethylformamide in the presence of N-ethyldiisopropyl-amine at room temperature to yield the 2-methyl-5-nitro-6-(4-phenyl-piperidin-1-yl)-3H-pyrimidin-4-one as yellowish solid; m.p. 210-213° C.; MS: [M+H]+=315.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673795B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-7c43274fc2fd49b08040c09d9a8f5558 |
| Source note | uspto-grants-2004_01 |