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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266054Generated: October 26, 2026

Dimethylformamide → HCID 21472338, compound

https://huagongshe.com/reaction/266054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12208484HCID 12208484—
Reactant1-(4-Bromophenyl) 2-heptyn-1-oneHCID 54449136—
SolventWaterHCID 962—
ProductHCID 21472338HCID 2147233845.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650414
Source datasetuspto-grants-1997_07
ORD IDord-ce923dd23ee64f87b8f674d49b86bcc9
Source noteuspto-grants-1997_07