HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266054Generated: October 26, 2026
Dimethylformamide → HCID 21472338, compound
https://huagongshe.com/reaction/266054
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12208484 | HCID 12208484 | — |
| Reactant | 1-(4-Bromophenyl) 2-heptyn-1-one | HCID 54449136 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21472338 | HCID 21472338 | 45.6% |
Reaction Steps
A mixture of 13.8 g of ethyl 1-aminopyridinium 3-carboxylate 2,4,6-trimethylbenzenesulphonate (compound A) (Synthesis 1977, page 1, TAMURA, et al.), 150 ml of dimethylformamide, 5.7 g of potassium carbonate and 10 g of the product of Step A of Example 1 were stirred for 3 hours at room temperature and then 6.9 g of compound A and 2.85 g of potassium carbonate were added. The mixture was stirred for 2 hours. Then 6.9 g of compound A and 2.85 g of potassium carbonate were added and the mixture was stirred for 2 hours at ambient temperature. The mixture was taken up in water and extracted with ethyl acetate. Separation was carried out by chromatography on silica (essence G: 80/ethyl acetate: 20) to obtain 7.38 g of the expected product (M.p.≤50° C.) and 8.25 g of the corresponding isomer of Example 16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650414 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-ce923dd23ee64f87b8f674d49b86bcc9 |
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| Source note | uspto-grants-1997_07 |
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