Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 69662067 | HCID 69662067 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178456587 | HCID 178456587 | 26% |
Reaction Steps
Compound 47a (70 mg, 0.158 mmol) obtained in Example 47 was dissolved in chloroform (2 mL), to the solution was added thionyl chloride (40 μL, 0.548 mmol, 3.4 equivalents), and the mixture was stirred at 60° C. for 30 minutes. To the reaction solution was added piperidine (320 μL, 3.24 mmol, 20 equivalents) and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated and directly purified by silica gel column chromatography (chloroform:methanol=98:2). Thereafter, the title compound (17 mg, 26%) was obtained in a manner similar to the method by which Compound 40 was obtained from Adduct 40a in Example 40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005430B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-4d2bea95749b4bda9d907ea7cf063c76 |
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| Source note | uspto-grants-2006_02 |
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