HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 57907147, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-chloro-N-hydroxybenzene-1-carbonimidoyl chloride | HCID 2755543 | — |
| Reactant | Ethyl 3-ethynylbenzoate | HCID 15540684 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 57907147 | HCID 57907147 | — |
Reaction Steps
In a 10 ml round flask, 500 mg (2.9 mmol) of 3-ethynyl-benzoic acid ethyl ester and 652 mg (3.5 mmol, 1.2 eq.) of 4-chloro-N-hydroxy-benzenecarboximidoyl chloride are dissolved in 4 ml of CHCl3. To this solution, 11 mg (0.14 mmol, 0.05 eq.) of pyridine and 290 mg (2.9 mmol) of triethyl amine are added at 0° C. under a nitrogen atmosphere. The orange solution is stirred under warming to room temperature for 20 h. The suspension is filtered and the solution concentrated in vacuo. Chromatographical purification (100 g SiO2; eluent: hexane/ethyl acetate 9:1) yields the title compound as a white solid. Mass spectrum: m/z (M+H)+: 328.2; 330.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432293B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-daba3c1af9284ba79c5d5e41ec0201fe |
| Source note | uspto-grants-2008_10 |