HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → (S)-2-amino-2-(3-fluoro-5-iodophenyl)ethyl di-tert-butyl phosphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | (9H-fluoren-9-yl)methyl piperidine-1-carboxylate | HCID 21896484 | — |
| Reactant | (S)-(9H-fluoren-9-yl)methyl (2-((di-tert-butoxyphosphoryl)oxy)-1-(3-fluoro-5-iodophenyl)ethyl)carbamate | HCID 118054603 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-2-amino-2-(3-fluoro-5-iodophenyl)ethyl di-tert-butyl phosphate | HCID 118045308 | — |
Reaction Steps
To (S)-(9H-fluoren-9-yl)methyl (2-((di-tert-butoxyphosphoryl)oxy)-1-(3-fluoro-5-iodophenyl)ethyl)carbamate (6450 mg, 9.27 mmol) was added DMF (Volume: 90 mL) followed by piperidine (25 mL, 253 mmol) and stirred at room temperature for 30 minutes, followed by LCMS. To the crude reaction mixture was added 750 ml of ethyl acetate, washed with saturated sodium bicarbonate (2×), water (5×), saturated salt solution, dried sodium sulfate, and filtered. The solvent was concentrated off to constant mass under high vacuum to give the desire crude product which includes FMOC piperidine impurity, used as is. LCMS (m/z): 474.2 (MH+), 0.80 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242996B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-19e6287ad4b94eaaa8dc70079e006e6c |
| Source note | uspto-grants-2016_01 |