Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trimethylphosphine | HCID 68983 | — |
| Reactant | HCID 86673850 | HCID 86673850 | — |
| Reactant | HCID 86673851 | HCID 86673851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68283529 | HCID 68283529 | — |
Reaction Steps
A mixture of (2R,3R,4R)-4-azido-2-benzylcarbamoyl-3-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester and (2S,3S,4S)-3-azido-2-benzylcarbamoyl-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester (3.52 g, 8.98 mmol) (described in Scheme B22), trimethylphosphine in THF (17.97 mL, 17.97 mmol) and water (0.32 mL, 17.97 mmol) in THF (100 mL) was stirred for 16 h at RT. The reaction mixture was quenched with water and extracted twice with EtOAc. The organic phases were joined, washed with brine, dried over Na2SO4, filtered and concentrated. Purification by flash column chromatography on silica gel (c-hexane/EtOAc 1:1) gave (2S,3S,4S)-3-amino-4-fluoro-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester: MS (UPLC/MS): 339 [M+H]+; tR (HPLC conditions f): 1.59 min and (2R,3S,4R)-4-amino-3-fluoro-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester: MS (UPLC/MS): 339 [M+H]+; tR (HPLC conditions f): 1.62 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09085555B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-b41baacf26c1418aa868688c226f747d |
|---|
| Source note | uspto-grants-2015_07 |
|---|