Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Chloro-6-fluorobenzothiazole | HCID 2049870 | — |
| Reactant | HCID 59385318 | HCID 59385318 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 59385209 | HCID 59385209 | — |
Reaction Steps
A mixture of methyl 4′-amino-3-chlorobiphenyl-4-carboxylate (0.45 g, 1.7 mmol) and 2-chloro-6-fluoro-1,3-benzothiazole (0.32 g, 1.7 mmol) in n-butanol (8 mL) was heated to 60-70° C., and then 4N HCl in 1,4-dioxane (0.19 mL, 0.77 mmol) was added dropwise with stirring. The reaction mixture was heated at 90° C. for 18 h. Upon cooling to rt, the reaction mixture was concentrated under reduced pressure. The residue was triturated with ethanol, and the solid was collected by filtration. This yielded 0.399 g (56%) of the title compound as a beige solid. LC/MS m/z 411 (MH+), retention time 4.03 min. 1H NMR (400 MHz, DMSO-d6) δ 3.85 (s, 3H), 7.12 (t, 1H), 7.67-7.87 (m, 9H), 10.62 (br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759376B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-06cb252c89e64f378dfbd54ea5666aad |
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| Source note | uspto-grants-2010_07 |
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