HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 22063255, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-Pyrimidin-2-yl-piperidin-4-one | HCID 1478856 | — |
| Reactant | HCID 22063255 | HCID 22063255 | — |
| Reactant | HCID 69416907 | HCID 69416907 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22063255 | HCID 22063255 | — |
| Product | HCID 22260486 | HCID 22260486 | — |
Reaction Steps
4-Amino-4-cyano-1-pyrimidin-2-yl-piperidine was prepared according to the procedure from Example 7, step a, starting with 1-(pyrimidin-2-yl)-4-piperidone with the exception that a 2 M ammonia in methanol solution replaced the 5 M ammonia in methanol solution. (b) The title compound was prepared starting from N-(4-Morpholinecarbonyl)-L-cyclohexyl alanine and 4-amino-4-cyano-1-pyrimidin-2-yl-piperidine according to the procedure from Example 2, step b, except that the compound was purified by HPLC using a 20×250 mm C18 reverse phase column with the method being 30% acetonitrile in water to 100% acetonitrile. MS, m/z 469=M+1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056915B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-6c880bf606d44839b11252a7baebe734 |
| Source note | uspto-grants-2006_06 |