Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 178488032 | HCID 178488032 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178488114 | HCID 178488114 | — |
Reaction Steps
To a mixture of 5-methoxy-2-mercaptobenzimidazole (1.673 g, 9.285 mmol) and p-xylyl bromide (1.718 g, 9.285 mmol) in DMF (33.5 mL) at 0° C., Cs2CO3 (4.53 g, 13.93 mmol) was added and the suspension was stirred for 24 h while being allow to warm from 0° C. to rt. Distilled water (150 mL) was added with vigorous stirring. The murky white suspension turned into a clearer solution with white granules. After being stirred for 20 min at rt, the mixture was filtered and the residue was rinsed with water (3×20 mL) and hexanes (3×20 mL). The crude product was >95% pure by 1H NMR analysis and was not further purified. The yield was 2.437 g, 92%. 1H NMR (500 MHz, CDCl3): δ 2.25 (s, 3H), 3.76/3.78 (app d*, 3H), 4.38/4.42 (app d*, 2H), 6.74-7.17 (m, 6H), 7.52 (d, 1H, J=7.5 Hz), 8.87 (brs, 1H); 13C NMR (125 MHz, CDCl3): δ 21.30, 37.39, 37.63, 55.89, 55.96, 94.15, 101.18, 110.39, 111.10, 112.45, 119.07, 128.98, 129.58, 133.94, 156.61. *The apparent doublets may arise from the 1,3-proton shift between the nitrogen atoms in the heterocycle.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710082B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-43a8da8813824252bccc22bd59c9e50c |
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| Source note | uspto-grants-2014_04 |
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