HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258470Generated: November 2, 2026
4-Hydroxy-N,N,2-trimethyl-1-((4-methylphenyl)sulfonyl)-1H-benzimidazole-6-carboxamide → 5-[(Dimethylamino)methyl]-4-hydroxy-N,N,2-trimethyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazole-6-carboxamide
https://huagongshe.com/reaction/1258470
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxy-N,N,2-trimethyl-1-((4-methylphenyl)sulfonyl)-1H-benzimidazole-6-carboxamide | HCID 67220315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[(Dimethylamino)methyl]-4-hydroxy-N,N,2-trimethyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazole-6-carboxamide | HCID 67220893 | — |
Reaction Steps
To a solution of 4-hydroxy-N,N,2-trimethyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazole-6-carboxamide (1.00 g, 2.68 mmol, Step 4) in dichloromethane (50 mL) was added N,N-dimethylmethyleneiminium iodide (545 mg, 2.95 mmol) at room temperature and the mixture was stirred at 40° C. for 15 hours. The reaction was quenched by saturated sodium hydrogencarbonate aqueous solution. The mixture was extracted with dichloromethane. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford the title compound as a yellow amorphous (1.04 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466166B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-94d618027daa474888184d89920ef7a1 |
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| Source note | uspto-grants-2013_06 |
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