Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15340372 | HCID 15340372 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18400197 | HCID 18400197 | 98.8% |
Reaction Steps
To a solution of 4-(4-(aminosulfonyl)phenyl)-5-(4-fluorophenyl)thiophene-2-carboxylic acid methyl ester (Example 1, Step 5) (0.210 g) in THF (2.0 mL) were added MeOH (1.0 mL), NaOH 1N (1.0 mL) and a few drops of NaOH 10N. The resulting mixture was heated at 45° C. for 2 h and the reaction was then partitioned between EtOAc and HCl (3N) to provide the title product as a white solid (0.200 g). 1H NMR (CD3COCD3) δ6.60 (2H, s), 7.15 (2H, t), 7.35 (2H, q), 7.45 (2H, d), 7.82 (2H, d), 7.87 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710140 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-7305150849c34073a12717eb5584545c |
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| Source note | uspto-grants-1998_01 |
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