HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178702Generated: November 1, 2026
3-Pyridyl isothiocyanate → HCID 178493489, compound
https://huagongshe.com/reaction/1178702
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Pyridyl isothiocyanate | HCID 2737242 | — |
| Reactant | (2,4,6-Trimethoxyphenyl)methyl 2-cyanoethanimidothioate | HCID 69515586 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178493489 | HCID 178493489 | 59% |
Reaction Steps
To compound 11 (6.76 g, 24.1 mmol) in ethyl acetate (18 mL) is added 3-pyridylisothiocyanate (3.9 ml-, 36.2 mmol) at room temperature. The reaction is then heated to 60° C. and stirred for 4 hours. More ethyl acetate is added (12 mL) and the reaction is stirred for an additional 4 hours. The reaction is cooled to room temperature and filtered. The solids are washed with ethyl ether twice and with methanol once. The solids are further dried in vacuo to obtain compound 12 (5.88 g, 59%). 1H NMR (d6 DMSO): δ 10.12 (1H, br. s), 8.46 (1H, d, J=2.4 Hz), 8.36 (1H, d, J=5.2 Hz), 7.71 (1H, d, J=9.0 Hz), 7.37 (1H, dd, J=9.0, 5.2 Hz), 6.27 (2H, s), 4.25 (2H, s), 3.81 (6H, s), 3.77 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276602B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-31acc6eb6d2c441c85721d86ea8a2734 |
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| Source note | uspto-grants-2007_10 |
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