HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (S)-4-(tert-butoxycarbonylamino)-5-methoxy-N,N,N-trimethyl-5-oxopentan-1-aminium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 58797552 | HCID 58797552 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-4-(tert-butoxycarbonylamino)-5-methoxy-N,N,N-trimethyl-5-oxopentan-1-aminium iodide | HCID 86702241 | — |
Reaction Steps
To a solution of (S)-methyl 2-(tert-butoxycarbonylamino)-5-(dimethylamino)pentanoate (5.62 g, 20.5 mmol, 1.0 eq) in THF (40 mL), was added iodomethane (1.4 mL, 22.5 mmol, 1.1 eq). The mixture was stirred at room temperature for 1 h, until the starting material was consumed as determined by LCMS analysis. The reaction mixture was concentrated and then dried under high vacuum to provide (S)-4-(tert-butoxycarbonylamino)-5-methoxy-N,N,N-trimethyl-5-oxopentan-1-aminium iodide as a white solid, which was used in the next step without purification. MS (EI) m/z 289 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846739B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-4de7ca38eed24be592498768e2f9f8cc |
| Source note | uspto-grants-2014_09 |