Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57378078 | HCID 57378078 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57378192 | HCID 57378192 | — |
Reaction Steps
3 N NaOH (0.1 mL) was added to 1-[2-(4-tert-butyl-benzenesulfonylamino)-5-chloro-phenyl]-5-methyl-1H-[1,2,3]triazole-4-carboxylic acid methyl ester (synthesized according to general procedure GG, 22 mg, 0.047 mmol) in THF and the resultant reaction mixture stirred at 60° C. overnight. The following day, the reaction mixture was concentrated to dryness and purified by preparative TLC to generate the title compound: MS (ES) M+H expected 449.1, found 449.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409909B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-b1deeba4f6c1406a969c78e28c81fabc |
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| Source note | uspto-grants-2016_08 |
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