HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946385Generated: October 31, 2026
N-Hydroxyacetamidine → N-(1-{[2-Chloro-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]methyl}-1H-pyrazol-3-yl)-2,6-difluorobenzamide
https://huagongshe.com/reaction/1946385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxyacetamidine | HCID 30926 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Methyl 4-chloro-3-[(3-{[(2,6-difluorophenyl)carbonyl]amino}-1H-pyrazol-1-yl)methyl]benzoate | HCID 59547941 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(1-{[2-Chloro-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]methyl}-1H-pyrazol-3-yl)-2,6-difluorobenzamide | HCID 59547977 | — |
Reaction Steps
To a solution of acetamide oxime (89 mg, 1.20 mmol, GFS chemicals) in ethanol (2 ml) was added 4A activated molecular sieves (418 mg) (pre-dried in the oven overnight) and then 21% sodium ethoxide in ethanol (0.2 ml, 0.536 mmol, Alfa Aesar). To the reaction mixture was added methyl 4-chloro-3-[(3-{[(2,6-difluorophenyl)carbonyl]amino}-1H-pyrazol-1-yl)methyl]benzoate (for a preparation see Intermediate 23)(105 mg, 0.259 mmol). The reaction was heated to reflux (100° C.) and stirred for 3 h under nitrogen. The reaction mixture was evaporated in vacuo and the residue dissolved in methanol (0.5 ml) and filtered through a hydrophobic frit. The residue was dissolved with DMSO (0.5 ml) and the sample was purified by MDAP on Sunfire C18 column using Acetonitrile-Water with a Formic acid modifier (Method B). The solvent was evaporated in vacuo to give the title compound as a white gum (6.1 mg);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399436B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-d0f332b905cd402c8c7614d7c25838a7 |
|---|
| Source note | uspto-grants-2013_03 |
|---|