HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604232Generated: October 29, 2026
Potassium Cyanide → 2-Cyano-6-isopropylaminobenzothiazole
https://huagongshe.com/reaction/604232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Chloro-6-isopropylaminobenzothiazole | HCID 67040698 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Cyano-6-isopropylaminobenzothiazole | HCID 67040205 | — |
Reaction Steps
Potassium cyanide (18 mg) and 2-chloro-6-isopropylaminobenzothiazole (18 mg) were dissolved in 1 ml DMSO and heated to 120° C. for 4 h. After cooling to room temperature, the reaction was poured into 0.2M potassium phosphate, pH 4.5. The aqueous layer was extracted with ethyl acetate three times, washed with water, and dried over sodium sulfate. The solvent was removed by rotary evaporation and the residue purified by silica gel chromatography (20% ethyl acetate in hexanes). 1H-NMR (d6-DMSO): δ 7.83 (d, 1H, J=9.2 Hz), 7.15 (d, 1H, J=2.4 Hz), 6.97 (dd, 1H, J=2.4, 8.8 Hz), 6.52 (bd, 1H, J=7.2 Hz), 3.61 (m, 1H), 1.15 (d, 6H, J=6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910087B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-a4c153b43fc143efb6e90b203613d592 |
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| Source note | uspto-grants-2011_03 |
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