Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 58092780 | HCID 58092780 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Trimethylaluminum | HCID 16682925 | — |
| Product | HCID 58092758 | HCID 58092758 | — |
Reaction Steps
Trimethylaluminum in toluene (2 M, 15.95 mmol) was added dropwise to a mixture of NH4Cl (15.95 mmol) in toluene (2 mL) at 0° C. with the formation of methane gas. The reaction mixture was allowed to warm to rt, stirred for a further 15 min and then slowly treated with a solution of (2S,3S)-3-azidomethyl-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid methyl ester (Stage 36.4) (7.98 mmol) in toluene (8 mL). Additional reagent prepared from NH4Cl (15.95 mmol) in toluene (2 mL) and trimethylaluminum in toluene (2 M, 15.95 mmol) at 0° C. was added after 18 h. After stirring for 44 h, the mixture was cooled to 0° C., quenched with 1M HCl and then washed with CH2Cl2 (3×). The aqueous phase was basified with a 1:1 saturated solution of NaHCO3/saturated solution of Rochelle's salt and extracted with THF (10×). The combined organic layers were dried (Na2SO4), filtered and concentrated. The residue was purified using a RediSep® silica gel column to afford the title compound as a yellow oil. HPLC: tR=2.50 min (method G); ESI-MS: [M+H]+ 274; TLC: Rf=0.26 (3:1 Hex/EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357707B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-be8dffe9c89b435cbcce129cee95793f |
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| Source note | uspto-grants-2013_01 |
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