HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499197Generated: October 26, 2026
Hydrochloric Acid → 4-[3-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-ureido]benzoic acid
https://huagongshe.com/reaction/499197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-[3-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-ureido]benzoic acid ethyl ester | HCID 59420894 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[3-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-ureido]benzoic acid | HCID 59420892 | — |
Reaction Steps
To a suspension of 4-[3-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-ureido]benzoic acid ethyl ester (0.24 g, 0.71 mmol) in ethanol (4 mL) is added 1 N aq. NaOH solution (2 mL) and the mixture is heated at 80° C. for 2 hours. Then, 1 N HCl is added until pH 6 and the mixture is diluted with ethyl acetate. The organic phase is washed once with aqueous sodium chloride solution and dried over magnesium sulfate, filtered and evaporated under reduced pressure to give 0.19 g (0.59 mmol), 83% as white solid. ES+(m/z) 317 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767674B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-103db95bea444ed98e22c21a965358de |
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| Source note | uspto-grants-2010_08 |
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