HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Bis(2-methoxyethyl)amino)sulfur trifluoride → (S)-3-azido-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| Reactant | trans-3-Azido-1-Boc-4-hydroxypyrrolidine | HCID 11128048 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-3-azido-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 86608831 | 60.5% |
Reaction Steps
37.1 To stirred, cooled (−78° C.) solution of 695 mg (3S,4S)-3-azido-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester (example 22.2) in 5 ml CH2Cl2 under an argon atmosphere were added 2.69 g bis(2-methoxyethyl)aminosulphur trifluoride (50% solution in THF). The dry ice bath was removed and the mixture was allowed to warm to r.t. and stirring was continued for 22 h. The mixture was poured into 10% aq. Na2CO3. The organic phase was washed with brine, dried (MgSO4), filtered and concentrated. The crude product was purified by chromatography (silica gel; gradient: cyclohexane->cyclohexane/EtOAc 3:2) to give 424 mg (S)-3-azido-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester as light yellow oil. MS 409.0 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820699B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-8d731baa95b54a3a9a9d499993623182 |
| Source note | uspto-grants-2010_10 |