HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-Chloro-1H-indole-2-carbonyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | 5-Chloro-1H-indole-2-carboxylic acid | HCID 82693 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Chloro-1H-indole-2-carbonyl fluoride | HCID 22593874 | — |
Reaction Steps
A solution of 5-chloro-1H-indole-2-carboxylic acid (10.0 g, 51.1 mmol) and pyridine (33.1 mmol) in acetonitrile was added to a solution of cyanuric fluoride (2.76 g, 20.4 mmol) in acetonitrile (total 340 mL) at 25° C. The reaction was followed by TLC on aliquots quenched with butylamine and appeared nearly complete at 1 hour. The mixture was poured onto ice, extracted with ether, dried (Na2SO4), and concentrated giving a solid which was used without purification (10.0 g, 99%). TLC of a butylamine-quenched aliquot showed some 5-chloroindole-2-carboxylic acid and the less polar N-butylamide. A sample was purified by chromatography on silica gel eluting with ethyl acetate-hexanes (50-100%) for characterization (16368-130-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297269B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-d5b3331c50964542b808b4b2db2d1cf3 |
| Source note | uspto-grants-2001_10 |