Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Carbamic acid, 4-pyridinyl-, phenyl ester | HCID 11401617 | — |
| Reactant | HCID 86638577 | HCID 86638577 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59175897 | HCID 59175897 | 14.1% |
Reaction Steps
Phenyl pyridin-4-ylcarbamate (0.461 mmol, 0.099 g) was added to a stirred solution of 2-(4-((4-(4-amino-3-fluorobenzyl)piperazin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (0.279 mmol, 0.139) in dioxane (7 mL) and mixture heated in a microwave reactor for 10 minutes at 130° C. Water (10 mL) was added to the reaction followed by dichloromethane (10 ml). The organic layer was separated, washed with water (3×10 mL), dried over magnesium sulphate and concentrated under reduced pressure. The residue was purified by preparative HPLC giving the title compound (0.023 g). MS (ESI) m/z 586.3 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357679B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-963215e5989e4710acc908a0d21473be |
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| Source note | uspto-grants-2013_01 |
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