HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-chlorophenyl)-N'-hydroxyethanimidamide → 4-({3-[3-(4-Chlorobenzyl)-1,2,4-oxadiazol-5-yl]-5-(4-ethylphenyl)piperidin-1-yl}carbonyl)-morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-chlorophenyl)-N'-hydroxyethanimidamide | HCID 249345 | — |
| Reactant | 5-(4-Ethylphenyl)-1-(morpholin-4-ylcarbonyl)piperidine-3-carboxylic acid | HCID 58002225 | — |
| Product | 4-({3-[3-(4-Chlorobenzyl)-1,2,4-oxadiazol-5-yl]-5-(4-ethylphenyl)piperidin-1-yl}carbonyl)-morpholine | HCID 58002524 | — |
Reaction Steps
69 mg (0.20 mmol) of 5-(4-ethylphenyl)-1-(morpholin-4-ylcarbonyl)piperidine-3-carboxylic acid (Example 38A) and 41 mg (0.22 mmol, 1.1 eq.) of 2-(4-chlorophenyl)-N′-hydroxyethanimidamide were reacted according to the General Method 1. Yield: 62 mg (63% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119663B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-892479faecf9402785c95774905fe161 |
| Source note | uspto-grants-2012_02 |