HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252341Generated: October 31, 2026
3-Methoxypropyne → HCID 23156218, compound
https://huagongshe.com/reaction/252341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxypropyne | HCID 69393 | — |
| Reactant | 5-bromo-3-iodo-1-methyl-1H-indazole | HCID 23156226 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 23156218 | HCID 23156218 | — |
Reaction Steps
A solution of 81.67 g of 5-bromo-3-iodo-1-methyl-1H-indazole in 750 ml of N,N-dimethylformamide and 335 ml of triethylamine is admixed at room temperature under argon with 25 ml of 3-methoxypropyne, 5.5 g of copper(I) iodide and 10 g of bis(triphenylphosphine)palladium(II) chloride, and subsequently heated to 60° C. After 1 hour, the reaction mixture is cooled to room temperature, diluted with water and extracted with ethyl acetate (4×). The combined organic phases are dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a yellow solid from the residue by means of flash chromatography (SiO2 60F). Rf=0.67 (2:1 EtOAc-heptane). Rt=4.42 (gradient I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868036B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-a8f90e61a1e54e63b8cd5e5ce3954a41 |
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| Source note | uspto-grants-2011_01 |
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