HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703500Generated: October 26, 2026
Sodium Hydroxide → 2-[2-(4-Methylpiperazin-1-yl)ethylthio] benzimidazole
https://huagongshe.com/reaction/703500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(2-Chloroethyl)-4-methylpiperazine hydrochloride | HCID 22127112 | — |
| Reactant | HCID 178527775 | HCID 178527775 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[2-(4-Methylpiperazin-1-yl)ethylthio] benzimidazole | HCID 22150395 | — |
Reaction Steps
Grams 2.2 2-mercapto-1H-benzimidazol and 2.4 g NaOH were dissolved in 40 ml 90% ethyl alcohol, then 3.5 g 1-(2-chloroethyl)-4-methylpiperazine hydrochloride were added thereto. The reaction mixture was refluxed for 2 hours, the solid precipitate removed by filtration, the limpid solution evaporated to dryness and the residue dissolved in chloroform and washed with water. The organic phase was made anhydrous, then evaporated to dryness and the residue chromatographed on a column eluting with chloroform, methyl alcohol, cyclohexane, ammonium hydroxide (68:15:15:0.2). The fractions which contained the product, were collected together and evaporated to dryness and the residue which was triturated with isopropyl ether, gave 0.65 g 2-[2-(4-methylpiperazin-1-yl)ethylthio] benzimidazole melting at 93°-95° C. (with a slight decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983620 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-e2729036770f4c149f76fc15dc39b9c6 |
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| Source note | uspto-grants-1991_01 |
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