Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 67097389 | HCID 67097389 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67097251 | HCID 67097251 | — |
Reaction Steps
To a solution of methyl 4′-[2-[(tert-butoxycarbonyl)-[(2R)-2-hydroxy-2-(3-pyridyl)ethyl]amino]ethyl]-3-(cyclohexyloxy)-4-biphenylcarboxylate in N,N-dimethylformamide were added imidazole and tert-butyldimethylchlorosilane at room temperature. After stirring at room temperature for 15 minutes and at 35° C. for 3.5 hours. The reaction mixture was poured into 0.05N hydrochloric acid at room temperature. The products were extracted with ethyl acetate. The combined extracts were washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was purified by silica gel column chromatography to give methyl 4′-[2-[(tert-butoxycarbonyl)[(2R)-2-[[tert-butyl(dimethyl)silyl]oxy]-2-(3-pyridyl)ethyl]amino]ethyl]-3-(cyclohexyloxy)-4-biphenylcarboxylate (11.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928264B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-1ea94213174a48ae992f179b7feb534d |
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| Source note | uspto-grants-2011_04 |
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