HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxonium, triethyl-, hexafluorophosphate(1-) (1:1) → (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxonium, triethyl-, hexafluorophosphate(1-) (1:1) | HCID 167684 | — |
| Reactant | Isoquinolin-3-Amine | HCID 311869 | — |
| Reactant | (S)-2-(tert-butoxycarbonyl(methyl)amino)-6-methoxy-6-oxohexyl 1H-imidazole-1-carboxylate | HCID 57947517 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate | HCID 57947397 | 58.2% |
Reaction Steps
To a solution of (S)-2-(tert-butoxycarbonyl(methyl)amino)-6-methoxy-6-oxohexyl 1H-imidazole-1-carboxylate (2 g, 5.4 mmol) in DCM (10 mL) was added a solution of triethyloxonium hexafluorophosphate (1.61 g, 6.5 mmol, 1.2 equiv.) in DCM (5 mL) dropwise at 0° C. The solution was warmed up to RT and stirred for 15 min. A solution of isoquinolin-3-amine (0.94 g, 6.5 mmol, 1.2 equiv.) in DCM (5 mL) was added. The solution was stirred for overnight. DCM was removed and the residue was purified on RP-HPLC using a mixture of acetonitrile and H2O to give (S)-methyl 5-(tert-butoxycarbonyl(methyl)amino)-6-(isoquinolin-3-ylcarbamoyloxy)hexanoate (1.4 g, 58%). LRMS (M+H+) m/z 446.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759374B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-4e5e4df921bd443290adcef0c6b1fe20 |
| Source note | uspto-grants-2014_06 |