HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-difluoro-N'-hydroxybenzenecarboximidamide → 1-({3-[3-(2,5-Difluorophenyl)-1,2,4-oxadiazol-5-yl]5-[4-(trifluoromethyl)phenyl]piperidin-1-yl}-carbonyl)piperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-difluoro-N'-hydroxybenzenecarboximidamide | HCID 4358160 | — |
| Reactant | 1-[(4-Cyanopiperidin-1-yl)carbonyl]-5-[4-(trifluoromethyl)phenyl]piperidine-3-carboxylic acid | HCID 58002332 | — |
| Product | 1-({3-[3-(2,5-Difluorophenyl)-1,2,4-oxadiazol-5-yl]5-[4-(trifluoromethyl)phenyl]piperidin-1-yl}-carbonyl)piperidine-4-carbonitrile | HCID 58002378 | — |
Reaction Steps
100 mg (0.244 mmol) of 1-[(4-cyanopiperidin-1-yl)carbonyl]-5-[4-(trifluoromethyl)phenyl]piperidine-3-carboxylic acid (Example 100A) and 46.2 mg (0.269 mmol) of 2,5-difluoro-N′-hydroxybenzenecarboximidamide (Example 74A) were reacted according to the General Method 1. Yield: 72.5 mg (54% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119663B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-13fd6fa30897458bae8badb7cd184334 |
| Source note | uspto-grants-2012_02 |