HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251333Generated: October 25, 2026
Triethylamine → 3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acid
https://huagongshe.com/reaction/251333
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-hydrazino-N-methoxy-4-methyl-benzamide | HCID 11615346 | — |
| Reactant | 3-[5-amino-4-(3-iodo-benzoyl)-pyrazol-1-yl]-N-methoxy-4-methyl-benzamide | HCID 11784820 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acid | HCID 11209438 | 25% |
Reaction Steps
To a stirred solution of 3-hydrazino-4-methyl-benzoic acid hydrochloride 2 (242 mg, 1.19 mmol, 1.0 eq) in 25 mL of ethanol was added 2-benzoyl-3-phenylamino-acrylonitrile 4 (296 mg, 1.19 mmol, 1.0 eq, preparation: Grothasu, Davis, J. Am. Chem. Soc., 58, 1334 (1936)) and triethylamine (161 μL, 1.19 mmol, 1.0 eq) and the mixture was heated to 65° C. All solids dissolved when temperature reached 65° C. After three hours, LC-MS indicates consumption of the hydrazine. The solids were filtered to provide 3-(5-amino-4-benzoyl-pyrazol-1-yl)-4-methyl-benzoic acid 5 (95 mg, 25%) as a beige solid: HPLC (4 minute gradient) tR 2.10 min;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863314B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-004e36b6428a4fcc9ba5ad06daf0e6a5 |
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| Source note | uspto-grants-2011_01 |
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