HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455148Generated: October 25, 2026
Methyl isothiocyanate → HCID 67027559, compound
https://huagongshe.com/reaction/455148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl isothiocyanate | HCID 11167 | — |
| Reactant | 2-(2-(4-Chlorophenyl)imidazo[1,2-a]pyridin-3-yl)acetohydrazide | HCID 67029159 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67027559 | HCID 67027559 | — |
Reaction Steps
A solution of 2-(2-(4-chlorophenyl)imidazo[1,2-α]pyridin-3-yl)acetohydrazide (0.1 g, 0.33 mmol) in EtOH (1 mL) was treated with isothiocyanatomethane (0.023 mL, 0.33 mmol) and refluxed for 3 h. The precipitated thiosemicarbazide was filtered and dissolved in concentrated sulfuric acid. The reaction mixture was stirred for 30 min at rt. The mixture was poured into cold water and the precipitated product was filtered in vacuo and washed with ditilled water. The crude product was recrystallized in EtOH to provide the title product as a yellow solid. M/e+ 356 for C17H15ClN5S (M+H)+; 1H-NMR (400 MHz, CDCl3) δ 8.15 (d, J=6.9 Hz, 1H), 7.71 (d, J=8.4 Hz, 2H), 7.63 (d, J=9.1 Hz, 1H), 7.45 (d, J=8.4 Hz, 2H), 7.22 (m, 2H), 6.84 (t, J=6.6 Hz, 1H), 4.65 (s, 2H), 2.98 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497278B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-888b828b65714ecd81476971290fd73e |
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| Source note | uspto-grants-2013_07 |
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