HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671664Generated: October 30, 2026
Hydrochloric Acid → Methyl 6-(4-(ethylsulfonyl)phenoxy)-2-pyridin-2-yl-1H-benzimidazole-5-carboxylate
https://huagongshe.com/reaction/1671664
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 2-[4-(ethylsulfonyl)phenoxy]-5-nitro-4-[(2-pyridinylcarbonyl)amino]benzoate | HCID 57433541 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 6-(4-(ethylsulfonyl)phenoxy)-2-pyridin-2-yl-1H-benzimidazole-5-carboxylate | HCID 57433643 | — |
Reaction Steps
Methyl 2-[4-(ethylsulfonyl)phenoxy]-5-nitro-4-[(2-pyridinylcarbonyl)amino]benzoate (7.46 g) was suspended in dimethylformamide (37 ml) and methanol (37 ml), and tin(II) chloride dihydrate (17.3 g) and concentrated hydrochloric acid (15 ml) were added to it, and stirred under heat at 80° C. for 40 minutes. The reaction liquid was restored to room temperature, and gradually added to an aqueous sodium hydrogencarbonate solution and neutralized. Ethyl acetate was added to it, and stirred at room temperature for 30 minutes, and the formed salt was taken out through filtration. The filtrate was washed with water and saturated saline water. After dried, the solvent was evaporated away to obtain the entitled compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994331B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-efce8ba978f24b90b5aa16abeb002c00 |
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| Source note | uspto-grants-2011_08 |
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