HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluorobenzoic acid → HCID 117704012, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluorobenzoic acid | HCID 9935 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | HCID 117703985 | HCID 117703985 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117704012 | HCID 117704012 | — |
Reaction Steps
A solution of 2-Amino-5-(4,4-difluoro-piperidine-1-sulfonyl)-thiophene-3-carboxylic acid amide (53 mg, 0.18 mmol), TEA (125 μL, 0.90 mmol), DMAP (7 mg, 0.054 mmol), 2-Chloro-1-methylpyridinium iodide (60 mg, 0.23 mmol) and 2-fluorobenzoic acid (33 mg, 0.23 mmol) in DCM is stirred at 80° C. overnight. The mixture is then diluted with DCM and washed with aqueous NaHCO3. The organic phase is isolated evaporated, and the residue is purified by preparative chromatography to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09382254B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-28eddfa377f34d0ab8e1dd3babac4025 |
| Source note | uspto-grants-2016_07 |