HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304748Generated: November 1, 2026
Chloroform → 4-Bromo-7-methyl-5-aminobenzimidazole
https://huagongshe.com/reaction/2304748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetramethyltin | HCID 11661 | — |
| Reactant | 4,7-Dibromo-5-aminobenzimidazole | HCID 18379891 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Product | 4-Bromo-7-methyl-5-aminobenzimidazole | HCID 18379833 | 29% |
| Product | 4,7-dimethyl-3H-benzimidazol-5-amine | HCID 18379861 | — |
Reaction Steps
A solution of 4,7-dibromo-5-aminobenzimidazole (1.5 g, 5.1 mmol) in 10 ml of DMF was transferred into pressure bottle under Ar2. To the solution was added tetramethyltin 3.6 ml, 20 mmol) and bis(triphenylphosphine) palladium(II) chloride (200 mg). The resulting reaction mixture was stirred at 140° C. for 24 h and concentrated in vacuo, yielding a dark oil which was subjected to column chromatography (40% EtOAC/CHCl3) to yield 0.34 g (1.5 mmol, 29%) of the desired product as well as 0.75 g of 4,7-dimethyl-5-aminobenzimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06436982B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-e4ab0645ddb7498cb398c74f0f9d61bd |
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| Source note | uspto-grants-2002_08 |
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