Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (2s)-1-(Benzyl{[(2r)-6-bromo-3,4-dihydro-2h-chromen-2-yl]methyl}amino)-3-phenoxy-2-propanol hydrobromide | HCID 69894008 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59060801 | HCID 59060801 | — |
Reaction Steps
The compound of Example 86 (5.0 g, 10.4 mmol) and imidazole (1.06 g, 15.6 mmol, 1.5 eq.) were dissolved in dichloromethane. tert-Butyldimethylsilylchloride (2.03 g, 13.5 mmol, 1,3 eq.) was added, and the mixture was stirred for 15 hours. Solids were removed by filtration, and the filtrate was concentrated in vacuo. The resulting oil was purified by flash chromatography on silica gel eluted with 90:10 hexanes/ethyl acetate. The title compound was obtained as a yellow oil (5.3 g, 85%): 1H NMR (300 MHz, CDCl3) δ7.30-7.26 (m, 5 H), 7.25-7.20 (m, 3 H), 7.09 (s, 1 H), 6.91 (t, 1 H), 6.80 (d, 2 H), 6.63 (d, 1 H), 4.07-4.00 (m, 2 H), 3.81 (s, 2 H), 3.73 (dd, 1 H), 2.88-2.77 (m, 2 H), 2.64-2.56 (m, 4 H), 1.96-1.90 (m, 1 H), 1.61-1.55 (m, 1 H), 0.85 (s, 9 H), 0.07 (s, 3 H), 0.04 (s, 3 H); MS m/z 596.3 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699860B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-e6c32866b9944e7686944ba15ca55ad9 |
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| Source note | uspto-grants-2004_03 |
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