HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846299Generated: November 2, 2026
4-Methylmorpholine → HCID 86659806, compound
https://huagongshe.com/reaction/1846299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Benzenamine, 4-(1-methylpropyl)- | HCID 121771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-Amino-5-methanesulfonylbenzoic acid | HCID 23069004 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86659806 | HCID 86659806 | — |
Reaction Steps
To a suspension of 2-amino-5-methanesulfonyl-benzoic acid (0.750 g, 3.48 mmol) in THF (50 mL) were added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.730 g, 3.83 mmol), 1-hydroxybenzotriazole (0.510 g, 3.83 mmol), and 4-methylmorpholine (0.380 g, 3.83 mmol). The reaction mixture was stirred at room temperature for 5 minutes and then 4-sec-butyl-aniline (0.780 g, 5.22 mmol) was added. The reaction mixture was stirred at room temperature for 16 hours. The solvent was evaporated in vacuo, water was added, and the product was extracted with ethyl acetate. The solvent was evaporated in vacuo and the residue was washed with ether to obtain 2-amino-N-(4-sec-butyl-phenyl)-5-methanesulfonyl-benzamide as white solid. Yield: 0.75 g (62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952021B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b465bb5322f24005a9d28031b87e70eb |
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| Source note | uspto-grants-2015_02 |
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