HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300976Generated: October 29, 2026
Triethylamine → N-tert.-butyl-2-dimethylaminocarbonyl-5-propionylamino-benzenesulfonamide
https://huagongshe.com/reaction/2300976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | 5-Amino-n-tert.-butyl-2-dimethylaminocarbonylbenzenesulfonamide | HCID 15240544 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-tert.-butyl-2-dimethylaminocarbonyl-5-propionylamino-benzenesulfonamide | HCID 15240547 | — |
Reaction Steps
0.85 g of 5-amino-N-tert.-butyl-2-dimethylaminocarbonyl-benzenesulfonamide (Example e) is dissolved in 3.5 ml of DMF at 0° C., and 0.28 g of propionyl chloride and 0.50 ml of triethylamine are added. After the mixture has been stirred at 5° C. for 1 hour, it is taken up in ethyl acetate and washed successively with dilute hydrochloric acid and water. After the mixture has been dried over MgSO4 and the organic phase has been concentrated, 0.60 g of a highly viscous substance, which is employed in subsequent reactions without further purification (Example k), is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498253B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-f2fe4e34ef194121a07c4ce8d286d137 |
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| Source note | uspto-grants-2002_12 |
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