HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969687Generated: November 4, 2026
Anthranilic Acid → 2-amino-N-(4-tert-butylphenyl)benzamide
https://huagongshe.com/reaction/969687
Participants
| Role | Name | HCID | Charge |
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| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-amino-N-(4-tert-butylphenyl)benzamide | HCID 335177 | — |
Reaction Steps
A mixture of 4-tert-butyl-phenylamine (5.8 mL, 36.5 mmol), 2-amino-benzoic acid (5.0 g, 36.5 mmol), TBTU (12.9 g, 40.2 mmol) and DIEA (6.7 mL, 40.2 mmol) in 5 mL of DMF was heated (50° C.) for 12 h in a sealed tube. The mixture was diluted with EtOAc and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (SiO2, 20% EtOAc/hexane) and crystallized from EtOH:H2O (3:1) to afford a yellow solid. MS (ES+): 269.4. (M+H)+. Calc'd for C17H20N2O-268.35.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307088B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-e6b994e230c646c7b02fd7b05b3621ba |
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| Source note | uspto-grants-2007_12 |
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