HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79099Generated: October 26, 2026
Cyanuric chloride → 4-tert-butyl-N-methyl-N-(3-(aminosulfonyl)phenyl)benzamide
https://huagongshe.com/reaction/79099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-(4-tert-butyl-N-methylbenzamido)benzenesulfonic acid | HCID 58988055 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-tert-butyl-N-methyl-N-(3-(aminosulfonyl)phenyl)benzamide | HCID 24855318 | — |
Reaction Steps
A solution of 3-(4-tert-butyl-N-methylbenzamido)benzenesulfonic acid (12 mg, 35 μmol), cyanuric chloride (7.0 mg, 40 μmol), and triethylamine (6.0 μL, 40 μmol) in acetone (0.5 mL) was sealed in a glass tube and heated in a microwave oven at 120° C. for 10 min. Concentrated ammonium hydroxide (150 μL) was added, and the reaction was stirred for 6 h. The reaction was filtered, and the filtrate was purified by preparative reverse phase HPLC using 10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA) to give 4-tert-butyl-N-methyl-N-(3-(aminosulfonyl)phenyl)benzamide. LC/MS: m/z 347.3 (M+H)+ at 2.86 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841483B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0cf14ec331364fe0a309edd917005dbb |
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| Source note | uspto-grants-2014_09 |
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