Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-(Benzoxazol-2-yl)benzyl bromide | HCID 11033515 | — |
| Reactant | HCID 54395449 | HCID 54395449 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15198019 | HCID 15198019 | — |
Reaction Steps
To KH (35%; (0.34 g; 0.0029 mole) in THF (8 ml) under N2 and cooled in an ice bath is added N-trityl-5-hydroxytricyclo-[3.3.1.13,7 ]decan-2-amine (1.0 g; 0.0025 mole) This forms a pale yellow solution and is stirred at room temperature for 1 hour. The reaction mixture is then cooled in ice and 4-(benzoxazol-2-yl)benzyl bromide (0.7 g; 0.0025 mole) is added all at once. The mixture is stirred for 1/2 hour with ice cooling and then 31/2 hours at room temperature then cooled in ice and MeOH is added to quench the KH. The mixture is evaporated to dryness. Purification is accomplished on HPLC eluting with a gradient system staring with 10% and ending with 20% ethyl acetate/hexane to obtain N-trityl-5-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7 ]decan-2-amine which is used directly in step F.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05596020 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-5fa2dd0866c642e48a6ba1f0bb23fe99 |
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| Source note | uspto-grants-1997_01 |
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