HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356811Generated: November 2, 2026
Methanol → 4'-[(6-Fluoro-1,3-benzothiazol-2-yl)amino]-3-chlorobiphenyl-4-carboxylic acid
https://huagongshe.com/reaction/2356811
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 59385209 | HCID 59385209 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-[(6-Fluoro-1,3-benzothiazol-2-yl)amino]-3-chlorobiphenyl-4-carboxylic acid | HCID 59385271 | — |
Reaction Steps
Methyl 4′-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-3-chlorobiphenyl-4-carboxylate (0.30 g, 0.71 mmol) was suspended in THF (5 mL), MeOH (5 mL) and water (2.5 mL), and then NaOH (0.28 g, 7.1 mmol) was added. The reaction mixture was heated at 50° C. for 3 h. Upon cooling to rt, the reaction mixture was concentrated under reduced pressure, acidified, and the resulting solid was collected by filtration. This yielded 0.34 g (quantitative) of the title compound. LC/MS m/z 399.2 (MH+), retention time 3.53 min.
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-f70a7edf0e7c47a9b12879a2ab8c0c5c |
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| Source note | uspto-grants-2010_07 |
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