HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2(N-methoxy-N-methylcarbamoyl)-3-methansulfonyloxypyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 57194245 | HCID 57194245 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2(N-methoxy-N-methylcarbamoyl)-3-methansulfonyloxypyrrolidine | HCID 86759849 | 138.8% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Methane sulphonyl chloride (3.49 g) was added dropwise over 10 minutes to a mixture of compound 65 (7.6 g) and triethylamine (7.7 ml) in dichloromethane (350 ml) and cooled to 0° C. under an argon atmosphere. It was then stirred at 0° C. for another hour. The reation mixture was then applied directly to a silica flash column which was eluted with ethyl acetate to give (2S,3 S)-1-tert-butoxycarbonyl)-2(N-methoxy-N-methylcarbamoyl)-3-methansulfonyloxypyrrolidine (compound 66) as a gum (9.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06946468B1 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-691c730c0dbb4d2c8591f51f8d5319e7 |
| Source note | uspto-grants-2005_09 |