HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222281Generated: October 30, 2026
Potassium Iodide → 5-[2-[4-(1H-indol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl]-2-methylthio-3,6-dimethyl-3H-pyrimidin-4-one
https://huagongshe.com/reaction/2222281
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole | HCID 2761023 | — |
| Reactant | 2-methylthio-5-(2-chloroethyl)-3,6-dimethyl-3H-pyrimidin-4-one | HCID 69316411 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-[2-[4-(1H-indol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl]-2-methylthio-3,6-dimethyl-3H-pyrimidin-4-one | HCID 11675590 | — |
Reaction Steps
To a solution of 3-(1,2,3,6-tetrahydropyridin-4-yl)indole (1.0 g, 5 mmol) in acetonitrile (30 ml) was added 2-methylthio-5-(2-chloroethyl)-3,6-dimethyl-3H-pyrimidin-4-one (1.42 g, 6.1 mmol), potassium iodide (0.84 g, 5 mmol) and triethylamine (1.4 ml, 10 mmol). The mixture was heated at 80° C. for 8 hours, cooled, concentrated and purified by flash chromatografy (dichloromethane/methanol/ammonia=95/4.5/0.5)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371769B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-7be1f198750b4418a2b3c94018e7365e |
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| Source note | uspto-grants-2008_05 |
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