Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67322062 | HCID 67322062 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67322152 | HCID 67322152 | 55% |
Reaction Steps
A mixture of 0.040 g (0.088 mmol) of N-{2-[4-(2-bromo-ethyl)-piperidin-1-yl]-5-chloro-phenyl}-3-chloro-benzamide, 0.044 g (0.44 mmol) of 4-hydoxypiperidine, and 0.50 mL (2.9 mmol) of N,N-diisopropylethylamine in acetonitrile (1 mL) is heated to 175° C. in a microwave reactor for 30 minutes. The mixture is cooled to room temperature and purified by preparative reverse phase HPLC to provide 0.023 g (55%) of the title compound (100) as a colorless solid. [M+H]+=476.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08952004B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-c1a3f4f76aad462a9256a7a2df68eecb |
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| Source note | uspto-grants-2015_02 |
|---|