HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16733Generated: October 25, 2026
Methyl 4-benzamidobenzoate → HCID 178490049, compound
https://huagongshe.com/reaction/16733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-benzamidobenzoate | HCID 727255 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 1-tert-butyl-3-(3-methoxyphenethyl)-1H-pyrazol-5-amine | HCID 57453934 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178490049 | HCID 178490049 | — |
Reaction Steps
5-[2-(3-Methoxyphenyl)ethyl]-2-tert-butyl-pyrazol-3-amine (0.2 g, 0.73 mmol) was dissolved in toluene (10 ml) and to this was added methyl 4-benzamidobenzoate (200 mg, 0.80 mmol) and AlMe3 (0.93 ml, 1.8 mmol). The reaction was stirred overnight. The reaction was diluted with DCM (15 ml) and quenched with damp sodium sulfite. The reaction mixture was stirred for 20 mins before being filtered and the solvent removed in vacuo to yield a yellow gum. This gum was dissolved in formic acid (12 ml) and heated at 82° C. overnight. The reaction was evaporated to dryness and the resulting product was passed through a SCX column, eluting initially with methanol followed by 2N ammonia/methanol. After removal of the solvent, a yellow solid was obtained which was triturated with hot acetonitrile to afford a white solid. The solid was filtered and dried (66 mg, 21%); 1H NMR (400.132 MHz, DMSO) δ 2.91 (s, 4H), 3.74 (s, 3H), 6.46 (brs, 1H), 6.77 (d, 1H), 6.83 (s, 2H), 7.20 (t, 1H), 7.64-7.54 (m, 3H), 7.90 (d, 2H), 8.02-7.97 (m, 4H), 10.46 (s, 1H), 10.55 (s, 1H), 12.15 (s, 1H); MS: m/z 441 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737149B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-9241a3d41e43465c9950e79544ff4838 |
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| Source note | uspto-grants-2010_06 |
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