HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276058Generated: October 26, 2026
Potassium Bicarbonate → N-benzenesulfonyl-4-acetylamino-3-(4-benzyloxybenzylamino)benzamide
https://huagongshe.com/reaction/276058
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 1-(Benzyloxy)-4-(bromomethyl)benzene | HCID 10492756 | — |
| Reactant | n-Benzenesulfonyl-3-amino-4-acetylaminobenzamide potassium salt | HCID 69689854 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzenesulfonyl-4-acetylamino-3-(4-benzyloxybenzylamino)benzamide | HCID 18681166 | — |
Reaction Steps
A mixture containing 0.500 g of N-benzenesulfonyl-3-amino-4-acetylaminobenzamide potassium salt, 0.470 g of 4-benzyloxybenzyl bromide, 0.925 g of a 20% potassium hydrogencarbonate aqueous solution and 3 ml of N,N-dimethylformamide was stirred at 90° C. for 1 hour. The reaction solution was concentrated, and was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and methanol at a ratio of 9:1) to obtain crude N-benzenesulfonyl-4-acetylamino-3-(4-benzyloxybenzylamino)benzamide. This crude product was cyclized in the same manner as in Example 183 to give 0.160 g of 6-benzenesulfonylcarbamoyl-1-(4-benzyloxybenzyl)-2-methylbenzimidazole (251).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352985B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-ad70cb05a23e43eca8c9b0b8efedb81e |
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| Source note | uspto-grants-2002_03 |
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