HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300790Generated: November 1, 2026
5-Aminobenzimidazole → HCID 15549643, compound
https://huagongshe.com/reaction/2300790
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Aminobenzimidazole | HCID 13623 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-2-methylthiopyrimidine | HCID 97113 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15549643 | HCID 15549643 | — |
| Product | HCID 15549644 | HCID 15549644 | — |
Reaction Steps
To a stirred solution of 5-aminobenzimidazole (700 mg, 5.26 mmol, 1 eq) in DMF (21 mL) was added NaH (231 mg, 5.78 mmol, 1.1 eq, (60% suspension in oil)). The mixture was allowed to stir until gas evolution ceased. To the DMF solution was added 2-methylthio-4-chloropyrimidine (0.612 mL, 5.26 mmol, 1 eq) dropwise via syringe. The mixture was allowed to stir overnight. The DMF was removed under reduced pressure and the residue was diluted with water and extracted 3× with CH2Cl2. The organic extracts were combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The mixture was purified by preparative thin layer chromatography (eluted 2× with 3.5% MeOH/CH2Cl2) to give 149 mg 2-methylthio-4-[6-aminobenzimidazol-1-yl]pyrimidine (faster regioisomer) and 89 mg 2-methylthio-4-[5-aminobenzimidazol-1-yl]pyrimidine (slower regioisomer).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498165B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-9626e77457fa46c8ac965fa3dc965d43 |
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| Source note | uspto-grants-2002_12 |
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