HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699641Generated: October 27, 2026
Methanol → N-1-butylsulfonyl-4-acetylamino-3-aminobenzamide
https://huagongshe.com/reaction/1699641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | N-(1-butanesulfonyl)-4-acetylamino-3-nitrobenzamide | HCID 18680978 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-1-butylsulfonyl-4-acetylamino-3-aminobenzamide | HCID 18681187 | 68.5% |
Reaction Steps
N-(1-butanesulfonyl)-4-acetylamino-3-nitrobenzamide (10.75 g) is dissolved with methanol (200 ml) and water (30 ml), and potassium bicarbonate (7.59 g) is added. The solution is hydrogenated with a 5% palladium/carbon (2.53 g) catalyst under a hydrogen environment for 24 hours at 40° C. The solids are separated through filtration, the residue, which is obtained by concentrating the filtrate, is purified using silica gel column chromatography (eluate: ethyl acetate/methanol=4/1), and 6.72 g of N-1-butylsulfonyl-4-acetylamino-3-aminobenzamide is obtained. 1H-NMR (DMSO-d6, δ): 0.86 (3H, t, J=7.3 Hz), 1.33-1.43 (2H, m), 1.59-1.67 (2H, m), 2.07 (3H, s), 3.37-3.43 (2H, t), 5.12 (2H, br s), 7.13 (1H, dd, J=8.2 and 2.0 Hz), 7.28 (1H, d, J=1.9 Hz), 7.40 (1H, d, J=8.3 Hz), 9.09 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06348032B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-2707e77c17f245619c113c215173249b |
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| Source note | uspto-grants-2002_02 |
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