Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | [(1S,2S)-2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hex-1-yl]-carbamic acid tert-butyl ester | HCID 69342316 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69336084 | HCID 69336084 | 98.9% |
Reaction Steps
To a flame dried 250 mL rbf equipped with a dry ice condenser was added fresh sodium metal (0.32 g, 14 mmol). The flask was immersed in a −78° C. bath and ammonia gas was condensed into the flask (˜30 mL). Racemic Intermediate 47, one enantiomer being [(1S,2S)-2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hex-1-yl]-carbamic acid tert-butyl ester (3.0 g, 7.0 mmol) in THF (7 mL, 2 mL rinse) was added to the flask in a fast dropwise fashion and the thick mixture was stirred for 5 minutes at which point tic indicated the reaction was complete. The reaction was warmed to room temperature and volatile solvents allowed to evaporate. The residue was partitioned between H2O and methylene chloride, the organics were washed with brine, dried over sodium sulfate, filtered, and concentrated to give the title compound as a foam (1.9 g, quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241798B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-5ae68806bb3b418193aff8ef7d20012c |
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| Source note | uspto-grants-2007_07 |
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