HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113066Generated: November 1, 2026
Potassium Cyanide → 6-Amino-2-cyanobenzothiazole
https://huagongshe.com/reaction/2113066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 2-Chloro-1,3-benzothiazol-6-amine | HCID 10921203 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Amino-2-cyanobenzothiazole | HCID 14157112 | 54% |
Reaction Steps
Potassium cyanide (1.29 g, 19.7 mmol) was added to dimethyl sulfoxide (DMSO, 150 mL). After argon substitution, the mixture was refluxed overnight at 135° C. with stirring. The temperature was lowered to 120° C., and Compound 3 (1.02 g, 5.55 mmol) dissolved in DMSO (20 mL) was added. After disappearance of the starting materials was confirmed by thin layer chromatography (developing solvent: ethyl acetate/n-hexane=2/1), the reaction mixture was poured into a mixed solution of 1.0 mol/L potassium dihydrogenphosphate solution (100 mL) and diethyl ether, (150 mL), and the diethyl ether layer was separated. The aqueous layer was extracted 5 times with ethyl acetate, the organic layer was mixed with the diethyl ether layer, and this organic solvent layer was washed twice with purified water and twice with saturated brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: ethyl acetate/n-hexane=1/4 to 1/2) to obtain Compound 4 as yellow solid (521 mg, 54% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524876B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-f7de2d01612043cc97bef0be7dd929a2 |
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| Source note | uspto-grants-2009_04 |
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