Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzyl-4-piperidinol | HCID 98152 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(2-Chloroethyl)-3-(2-methylquinolin-4-yl)urea | HCID 2344366 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Palosuran | HCID 10173280 | — |
Reaction Steps
To a solution of 4-hydroxy-4-benzyl-piperidine (380.6 mg, 2 mmol) in dry THF (10 mL) is added 1-(2-chloro-ethyl)-3-(2-methyl-quinolin-4-yl)-urea (263.7 mg, 1 mmol) and solid NaHCO3 (672 mg, 8 mmol). The reaction mixture is stirred at 45° C. for 6 days. The reaction mixture is diluted with CH2Cl2 (100 mL) and washed with sat. Na2CO3 (2×30 mL). The aqueous phase is re-extracted with CH2Cl2 (2×25 mL), the combined organic phases are washed with brine (20 mL), dried (Na2SO4), filtered and evaporated. The residue is purified by preparative HPLC to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07375227B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-a7135f3aee1c4ce9b0a672eb0e1b3c3f |
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| Source note | uspto-grants-2008_05 |
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