HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033741Generated: October 30, 2026
Water → 2-[(4-Difluoromethoxy-3-methyl-2-pyridyl)methylthio]benzimidazole
https://huagongshe.com/reaction/1033741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 178431607 | HCID 178431607 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(4-Difluoromethoxy-3-methyl-2-pyridyl)methylthio]benzimidazole | HCID 15230232 | — |
Reaction Steps
In N,N-dimethylforamide (DMF) (100 ml) was dissolved 2-[(4-hydroxy-3-methyl-2-pyridyl)methylthio]benzimidazole (10.5 g). To the solution was added 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU) (7.1 g), to which was introduced chlorodifluoromethane for 3 hours at room temperature. The reaction mixture was poured into water (500 ml), which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off. The residue was subjected to a silica gel column chromatography. From the portion eluted with chloroform-methanol (100:1, v/v), 2-[(4-difluoromethoxy-3-methyl-2-pyridyl)methylthio]benzimidazole was obtained (2.5 g, 20%). Recrystallization from ethyl acetate - hexane gave colorless needles, m.p. 99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05312824 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-799d56d44e894c2bb11d33083a3da714 |
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| Source note | uspto-grants-1994_05 |
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