Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-tert-Butoxycarbonylaminopropyl methanesulfonate | HCID 14427184 | — |
| Reactant | 4-[4-(Benzyloxy)phenoxy]phenol | HCID 14692699 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86761885 | HCID 86761885 | — |
Reaction Steps
4-(4-Benzyloxyphenoxy)phenol (1.948 g, 6.66 mmol), 2-tert-butoxycarbonylaminopropyl methanesulfonate (2.0 g, 6.66 mmol) and cesium carbonate (5.43 g, 16.66 mmol) were stirred in 75 ml of DMF at 80° C. for 3 h. Following addition of 2 g of 2-tert-butoxycarbonylaminopropyl methanesulfonate the reaction mixture was stirred at 80° C. for a further 4 h. The reaction mixture was concentrated in vacuo and the residue is taken up in ethyl acetate and water. The organic phase was separated off, concentrated and the residue was purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 837 mg (28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470841B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-655edb3832e0497694695e8112c38dc2 |
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| Source note | uspto-grants-2013_06 |
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