HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975156Generated: November 2, 2026
Sodium borohydride → HCID 18920285, compound
https://huagongshe.com/reaction/1975156
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(4-(2-(2-Ethoxyethoxy)ethoxy)-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide | HCID 19075326 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18920285 | HCID 18920285 | — |
Reaction Steps
Sodium borohydride (230 mg, 6 mmol) was added to a solution of 3-(4-(2-(2-ethoxyethoxy)ethoxy)-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide (3 mmol) in ethanol (99.9%, 20 ml) and the reaction mixture was stirred at -10° C. for 1 h. After evaporation the residue was dissolved in water and extracted with ethyl acetate. The dried organic phases were evaporated and the residue purified by column chromatography (SiO2, eluent: ethyl acetate/methanol (4:1)). The title compound was crystallized as the oxalate salt from acetone to yield 290 mg. (M.p. 115°-116° C.; M+ : 313; Compound 43).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05284859 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-c1311019a7714f4cac81dd9d2818539e |
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| Source note | uspto-grants-1994_02 |
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