Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | (1-Ethoxycyclopropoxy)trimethylsilane | HCID 2734686 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 53629854 | HCID 53629854 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66674145 | HCID 66674145 | 56.2% |
Reaction Steps
Dissolve (R)-1-(5-bromo-pyridin-2-yl)-pyrrolidin-3-ylamine (1.60 g, 6.63 mmol) in CH3OH (915 mL). Add (1-ethoxy-cyclopropoxy)-trimethyl-silane (2.7 mL, 13.49 mmol) and HOAc (1.9 mL, 33.15 mmol) and stir at RT for 3 h. Add NaBH3CN (4.2 g, 66.30 mmol) and reflux overnight. Cool the mixture to 0° C., quench with 2.0 M NaOH (15 mL), and dilute with H2O (100 mL). Extract with EtOAc (3×100 mL). Wash the combined organic layers with 1.0 M NaOH (50 mL), H2O (100 mL), and brine (50 mL). Dry the solution with Na2SO4, filter, and concentrate. Purify the crude material by chromatography, eluting with 0.5% Et3N, 5% CH3OH and 95% CHCl3 to give 1.20 g (56%) of the title compound. MS/ES m/z (79Br) 322 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101764B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-38f2f760ba0b4edfb0065174a5ca6a2a |
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| Source note | uspto-grants-2012_01 |
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