Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 67285368 | HCID 67285368 | — |
| Product | HCID 67285881 | HCID 67285881 | — |
Reaction Steps
The compound (102 mg) obtained in Example 5(1) was dissolved in methanol (1 mL) and, furthermore, thionyl chloride (0.25 mL) was added at 0° C. The reaction solution was stirred at 60° C. for 1 hour. The reaction solution was concentrated under reduced pressure and the residue was purified by silica gel chromatography (manufactured by Fuji Silysia Chemical Ltd., CHROMATOREX NH (trade name)) (dichloromethane:methanol=1:0→4:1) to obtain the title compound (96.4 mg) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476290B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e85a94103c0d47b8a0948fab337b92bf |
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| Source note | uspto-grants-2013_07 |
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