HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (S)-2-Amino-2-cyclohexyl-1-{(S)-2-[2-(1H-indole-3-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | ((S)-1-Cyclohexyl-2-{(S)-2-[2-(1H-indol-3-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester | HCID 66889931 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-Amino-2-cyclohexyl-1-{(S)-2-[2-(1H-indole-3-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-ethanone | HCID 66889854 | — |
Reaction Steps
A solution of ((S)-1-Cyclohexyl-2-{(S)-2-[2-(1H-indol-3-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester (120 mg, 0.24 mmol) in DCM (2 mL) is added TFA (2 mL). After stirring at room temperature for 1 h, the reaction mixture is concentrated down to give crude (S)-2-Amino-2-cyclohexyl-1-{(S)-2-[2-(1H-indole-3-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-ethanone, which is used in next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044209B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-c6077160a4f6488894450aad69e63f99 |
| Source note | uspto-grants-2011_10 |