HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-BOC-3(R)-methoxy-(L)-proline, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,2-Pyrrolidinedicarboxylic acid, 3-hydroxy-, 1-(1,1-dimethylethyl) 2-methyl ester, (2R,3S)-rel- | HCID 10988545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-BOC-3(R)-methoxy-(L)-proline, methyl ester | HCID 66619640 | 94.1% |
Reaction Steps
To a solution of 500 mg (2.05 mmol) of N-BOC-3(R)-hydroxy-(L)-proline, methyl ester and 1.7 g (12.2 mmol) of MeI in 10 mL of DMF was added 473 mg (2.05 mmol) of Ag2O. The mixture was stirred for 18 h and was then filtered through a pad of celite and concentrated. The crude residue was dissolved in EtOAc and washed with 1M HCl (2×10 mL), saturated NaHCO3 (2×10 mL), brine (1×10 mL), dried anhydrous MgSO4, and concentrated to give 500 mg of N-BOC-3(R)-methoxy-(L)-proline, methyl ester as a light yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943180B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-d5da4b881a2e45be924d91c64f08c5ad |
| Source note | uspto-grants-2005_09 |