Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Methylhomopiperazine | HCID 228349 | — |
| Reactant | HCID 11063100 | HCID 11063100 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 9816704 | HCID 9816704 | 98.4% |
Reaction Steps
A 25 ml 3-necked flask equipped with a condenser and magnetic stirring bar and under a nitrogen atmosphere was charged with a solution of N-methylhomopiperazine (0.35 ml; 2.81 mmol) in DMAC (10 ml). Potassium iodide (0.1 g) was added followed by the addition of 4-chloro-3,4-dihydro-2H-benzothiopyran (0.20 g; 1.2 mmol). This solution was then heated at 60° C. overnight, cooled, and partitioned between water and ethyl acetate which was washed with brine and dried with magnesium sulphate. Filtration and evaporation of solvent gave a yellow oil which was distilled by kugelrohr to give the title compound as an oil (0.31 g), bp (air bath temperature) 130-140° C. at 100 mtorr; essentially homogeneous by tlc (silica gel, 89:10:1 CH2Cl2:CH3OH:NH4OH), Rf 0.46; 1H nmr δ2.37 (s, 3H), 3.82-3.87 (m, 1H), 6.98-7.34 (m, 3H), 7.69-7.71 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06407093B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-09f6e3aaa2ac424ea75e1f4fa9b54970 |
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| Source note | uspto-grants-2002_06 |
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