HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → ((R)-3-Aminopyrrolidin-1-yl)(3-(methylsulfinyl)-1-(5-phenylpyrimidin-2-yl)-1H-indol-6-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl ((3R)-1-(3-(methylsulfinyl)-1-(5-phenylpyrimidin-2-yl)-1H-indole-6-carbonyl)pyrrolidin-3-yl)carbamate | HCID 131735398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ((R)-3-Aminopyrrolidin-1-yl)(3-(methylsulfinyl)-1-(5-phenylpyrimidin-2-yl)-1H-indol-6-yl)methanone | HCID 118666238 | — |
Reaction Steps
A 4M solution of TFA in dichloromethane (5.22 mL, 20.91 mmol) was added to 223d) (0.28 g, 0.52 mmol) in dichloromethane (16 mL) and the resulting mixture was stirred at room temperature for 3 h. The solution was concentrated, diluted with dichloromethane (40 mL), then washed with saturated potassium carbonate solution (2×20 mL) and dried over sodium sulfate. After evaporation of the solvent, the remnant was triturated with ether, pentane and acetone. Light yellow solid. Yield: 0.11 g (46% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315490B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-b11d652a7a4348aeae1831b84fef259d |
| Source note | uspto-grants-2016_04 |