Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Reactant | HCID 86619632 | HCID 86619632 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11516307 | HCID 11516307 | — |
Reaction Steps
To a suspension of macroporous cyanoborohydride (102 mg, 2.35 mmol/g) in acetonitrile (0.5 mL), was added piperidine (19 μL), acetic acid (0.1 mL), and a solution of 4-(3-oxo-propyl)-6-(3-trifluoromethylphenyl)-pyrimidine-2-carbonitrile (49 mg) in acetonitrile (0.5 mL). The mixture was heated in the microwave at 150° C. for 10 min, filtered in a fritted tube using a Vacmaster multi-filtration apparatus, and purified by preparative-HPLC. 4-(3-Piperidin-1-yl-propyl)-6-(3-trifluoromethylphenyl)-pyrimidine-2-carbonitrile was isolated as a clear gum (12 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589095B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-3ccf0e01aa2b4fdc877862011b28368d |
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| Source note | uspto-grants-2009_09 |
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