HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271039Generated: October 25, 2026
1-Ethyl-4-ethynylbenzene → 4-Chloro-2-diisopropylaminomethyleneamino-5-(4-ethylphenylethynyl)pyrimidine
https://huagongshe.com/reaction/1271039
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-4-ethynylbenzene | HCID 142425 | — |
| Reactant | 4-Chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidine | HCID 73446451 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Chloro-2-diisopropylaminomethyleneamino-5-(4-ethylphenylethynyl)pyrimidine | HCID 73446450 | 63.7% |
Reaction Steps
A mixture of 6.3 g of 4-chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidine, 33 mL of triethylamine, 2.43 g of 4-ethyl-1-ethynylbenzene, 0.304 g of dichlorobis(triphenyl)phosphine palladium II and 0.21 g copper iodide was magnetically stirred at reflux temperature for 1.5 hrs. The mixture was filtered and the filtrate evaporated in vacuo. Both the precipitate and the evaporated filtrate were dissolved in dichloromethane and washed with water, dried over sodium sulfate, filtered and evaporated. The residues were dissolved in 1:1 dichloromethane-hexanes and separately purified by column chromatography. After initial elution with 1:1 dichloromethane-hexanes, the product was obtained by elution with dichloromethane and 50% ethyl acetate-dichloromethane. Evaporation of the eluates gave 4.04 g of 4-chloro-2-diisopropylaminomethyleneamino-5-(4-ethylphenylethynyl)pyrimidine as a thick amber syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205297B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-00d218d8dd114839b00fe84d3161ce11 |
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| Source note | uspto-grants-2007_04 |
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