HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[(4-Hydroxypiperidin-1-yl)carbonyl]-5-[4-(2,2,2-trifluoroethyl)phenyl]piperidine-3-carboxylic acid → (4-Hydroxypiperidin-1-yl) {3-(3-isopropoxy-1,2,4-oxadiazol-5-yl)-5-[4-(2,2,2-trifluoroethyl)-phenyl]piperidin-1-yl}methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[(4-Hydroxypiperidin-1-yl)carbonyl]-5-[4-(2,2,2-trifluoroethyl)phenyl]piperidine-3-carboxylic acid | HCID 58116504 | — |
| Reactant | isopropyl N-hydroxyimidocarbamate | HCID 76225143 | — |
| Product | (4-Hydroxypiperidin-1-yl) {3-(3-isopropoxy-1,2,4-oxadiazol-5-yl)-5-[4-(2,2,2-trifluoroethyl)-phenyl]piperidin-1-yl}methanone | HCID 58116553 | — |
Reaction Steps
According to General Method 1, 150 mg (0.362 mmol) of the compound from Example 58A and 62.7 mg (0.398 mmol, purity 75%) of isopropyl N′-hydroxyimidocarbamate [G. Zinner, G. Nebel, Arch. Pharm. 1970, 303, 385-390] were reacted. Yield: 41.6 mg (23% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084469B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-fa20f59acb514f7a926a4f89e12edbe3 |
| Source note | uspto-grants-2011_12 |