HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58109609, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 58109230 | HCID 58109230 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58109609 | HCID 58109609 | 98.8% |
Reaction Steps
To a solution of (R)-3-((S)-1-cyclohexylethyl)-6-(4-fluorophenyl)-6-(3-hydroxy propyl)-1,3-oxazinan-2-one (200 mg, 0.55 mmol) in CH2Cl2 (10 mL) was added Et3N (290 mg, 2.87 mmol) and MsCl (196 mg, 1.72 mmol) at 0° C. The reaction solution was stirred at rt for 2 h. The reaction was quenched by H2O and extracted with CH2Cl2. The organic phase was concentrated to give the 3-((R)-3-((S)-1-cyclohexylethyl)-6-(4-fluorophen-yl)-2-oxo-1,3-oxazinan-6-yl)propyl methanesulfonate (240 mg, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575156B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-baae95312fdf4576b2b22fa24d83ab50 |
| Source note | uspto-grants-2013_11 |