Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178460520 | HCID 178460520 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 178458084 | HCID 178458084 | — |
Reaction Steps
A mixture of (3S)-3-[(tert-butoxycarbonyl)amino]-3-(5-tert-butyl-1H-benzimidazol-2-yl)-2-methylpropanoic acid (Preparation 30, 7.25 g, 19.33 mmol), Boc2O (5.9 g, 27.0 mmol), pyridine (1 mL) and NaHCO3 (2 g, 25 mmol) in THF/DMF (200 mL/100 mL) was stirred at room temperature for 18 hours. 0.5M Ammonia in dioxane (150 mL) was added and the reaction continued stirring at room temperature for a further 18 hours. The reaction was concentrated to dryness and diluted with saturated aqueous NaHCO3 solution. The solution was extracted with 2-MethylTHF and concentrated in vacuo. The residue was purified using reverse phase column chromatography eluting with 5-70% acetonitrile in 0.1% formic acid in water to afford the title compound as a mixture of diastereomers (3 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927587B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-00a03b1021054958b6a86a5a69b9e8ed |
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| Source note | uspto-grants-2015_01 |
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