HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 20740230, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1H-Indole-2-carboxylic acid, 1-methyl- | HCID 27695 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 86759485 | HCID 86759485 | — |
| Product | HCID 20740230 | HCID 20740230 | 81% |
Reaction Steps
To a solution of 1-methyl-1H-indole-2-carboxylic acid [((1S,2R)-2-((S)-1-cyano-3-methylsulfanyl-propylcarbamoyl)-cyclohexyl]-amide (compound 3-2, 203 mg, 0.492 mmol) in 20 mL of THF, was added Oxone™ (390 mg, 0.634 mmol). The reaction mixture was stirred at ambient temperature for 2 hours, filtered through a pad of celite, dried with sodium sulfate, filtered, concentrated, and purified by column chromatography (5:95, MeOH/CH2Cl2) to give 178 mg (81%) of 1-methyl-1H-indole-2-carboxylic acid [(1S,2R)-2-((S)-1-cyano-3-methanesulfonyl-propylcarbamoyl)-cyclohexyl]-amide as a yellow amorphous solid. MS: 445 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06759428B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-3833c16e22494857a3f13a1ba44789f5 |
| Source note | uspto-grants-2004_07 |