HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368632Generated: October 30, 2026
4-tert-Butylbenzenesulfonamide → HCID 22282042, compound
https://huagongshe.com/reaction/1368632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylbenzenesulfonamide | HCID 222872 | — |
| Reactant | HCID 22281998 | HCID 22281998 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 22282042 | HCID 22282042 | 33.6% |
Reaction Steps
A solution of 3-methoxy-4-(2-methoxyphenoxy)-1-methyl-1H-pyrazol-5-amine (Preparation 68) (45 mg), (4-tert-butyl)benzenesulfonamide (42 mg) and 4-dimethylaminopyridine (22 mg) in dry pyridine (2 ml) was stirred at room temperature for 16 hours. A further aliquot of (4-tert-butyl)benzenesulfonamide (42 mg) was added to the reaction mixture and stirring at room temperature was continued for a further 24 hours. The reaction mixture was diluted with ethanol (2 ml) and 1.0M aqueous sodium hydroxide solution (4 ml) and was then stirred at room temperature for 4 hours. The mixture was diluted with aqueous 1.0M hydrochloric acid (20 ml) and then extracted with ethyl acetate (3×15 ml). The combined organic extracts were washed with aqueous 1.0M hydrochloric acid (20 ml), dried (magnesium sulfate) and then concentrated under vacuum. The residue was purified by chromatography on silica (5 g) using 40% ethyl acetate/pentane as eluant to give the title compound as an off-white solid (27 mg), Rf 0.85 (ethyl acetate), m.p. 187.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06573270B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-dcb053b6797a49d58799a8ec6cab2d7b |
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| Source note | uspto-grants-2003_06 |
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