HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300975Generated: October 30, 2026
Formic Acid → N-tert.-butyl-2-dimethylaminocarbonyl-5-formylaminobenzenesulfonamide
https://huagongshe.com/reaction/2300975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Amino-n-tert.-butyl-2-dimethylaminocarbonylbenzenesulfonamide | HCID 15240544 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-tert.-butyl-2-dimethylaminocarbonyl-5-formylaminobenzenesulfonamide | HCID 15240546 | — |
Reaction Steps
A mixture of 0.34 ml of formic acid and 0.70 ml of acetic anhydride is heated at 50° C. for 2 hours, and a solution of 0.85 g of 5-amino-N-tert.-butyl-2-dimethylaminocarbonyl-benzenesulfonamide (Example e) and 3.5 ml of dimethylformamide (DMF) is added. After 4 hours, the mixture is taken up in ethyl acetate and washed successively with dilute hydrochloric acid and saturated NaHCO3 solution. After the mixture has been dried over MgSO4 and the organic phase has been concentrated, 0.88 g of a highly viscous substance, which is used in subsequent reactions without further purification (Example j), 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-2f2d58adfdf947618250318f4f46afef |
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| Source note | uspto-grants-2002_12 |
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