HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402091Generated: October 30, 2026
p-Chlorothiophenol → HCID 68006691, compound
https://huagongshe.com/reaction/2402091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 66749558 | HCID 66749558 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68006691 | HCID 68006691 | 76% |
Reaction Steps
N-(4-{4-bromo-3-cyano-5-[1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazol-3-yl]-2-thienyl}pyridin-2-yl)acetamide (0.2601 g, 0.5495 mmol), copper(I) oxide (0.1572 g, 1.099 mmol), 4-chlorobenzenethiol (0.3179 g, 2.198 mmol) and potassium carbonate (0.2278 g, 1.648 mmol) were added to a microwave vial followed by DMF (15.00 mL). The reaction was irradiated at 150° C. for 15 mins. The solid was filtered and washed with DCM. The solution was diluted with 80 ml water, and extracted with 100 ml DCM for two times. The organic layer was concentrated, and purified by column. The eluent was 50-100% ethyl acetate in hexane to yield a solid product (0.224 g, yield 76.0%) LCMS: (AA) ES+ 537, 539. 1H NMR (300 MHz, CDCl3) δ: 8.59 (s, 1H), 8.37 (d, 1H), 8.36 (s, 1H), 8.03 (s, 1H), 7.53 (d, 1H), 7.32 (d, 2H), 7.22 (d, 2H), 5.50-5.55 (dd, 1H), 4.02-4.08 (m, 1H), 3.68-3.78 (m, 1H), 2.25 (s, 3H), 2.10-2.18 (m, 1H), 2.00-2.07 (m, 2H), 1.66-1.80 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796271B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-47e4b19cfa794ca8979b177381586b66 |
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| Source note | uspto-grants-2014_08 |
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