HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylpiperidine → HCID 10155294, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18753232 | HCID 18753232 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10155294 | HCID 10155294 | — |
Reaction Steps
In analogy to the procedure described in example 20b, 4,6-dichloro-2-(2-hydroxy-ethylamino)-pyrimidine-5-carbonitrile (example 41a) was treated with 4-phenyl-piperidine in dioxane in the presence of N-ethyl-diisopropylamine at room temperature to yield 4-chloro-2-(2-hydroxy-ethylamino)-6-(4-phenyl-piperidin-1-yl)-pyrimidine-5-carbonitrile as an amorphous, white solid; MS: [M+H]+=358.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673795B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-c708e9fdfaae49819b742b44bc4c1f19 |
| Source note | uspto-grants-2004_01 |