HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412360Generated: October 25, 2026
4-Toluenesulfonyl chloride → N-(7-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]naphthalen-1-yl)-4-methylbenzenesulfonamide
https://huagongshe.com/reaction/412360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione | HCID 9832711 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(7-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]naphthalen-1-yl)-4-methylbenzenesulfonamide | HCID 18537695 | 27% |
Reaction Steps
A mixture of 5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione (0.4 g), p-toluenesulfonyl chloride (0.30 g), triethylamine (0.16 g) and anhydrous tetrahydrofuran (8 ml) was stirred at 50° C. for 5 hours and then at 70° C. for 2 hours. The reaction mixture was concentrated. To the residue was added water and the precipitate was washed with water and tetrahydrofuran to afford the title compound (0.14 g, mp 137-144° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562849B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-7bd8e515e1ed4f0b9e6f35b458e77261 |
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| Source note | uspto-grants-2003_05 |
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