Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 66801411 | HCID 66801411 | — |
| Product | HCID 86669010 | HCID 86669010 | — |
Reaction Steps
A stirred suspension of 2,6-dichloro-N-(3,5-difluoropyridin-4-yl)-benzamide (14.5 g, 47.8 mmol) in thionyl chloride (130 mL) was heated at 85° C. for 20 hours and then at 90° C. for 26 hours under argon. After cooling to room temperature, the volatiles were removed under reduced pressure, azeotroped with toluene (×3) to afford the title compound as a yellow solid (15.7 g, quantitative). LCMS (Method D): RT=4.16 min, m/z: 321 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697708B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-7b88d9fc32424f1eaf57b4e05a9287b0 |
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| Source note | uspto-grants-2014_04 |
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