HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875196Generated: October 31, 2026
(2R)-but-3-yn-2-ol → HCID 178462269, compound
https://huagongshe.com/reaction/1875196
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2R)-but-3-yn-2-ol | HCID 638102 | — |
| Reactant | HCID 178522959 | HCID 178522959 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178462269 | HCID 178462269 | 23.2% |
Reaction Steps
To a solution of N-({3-[(3-bromo-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)-4-chloro-1H-imidazole-5-carboxamide (70 mg, 0.142 mmol), palladiumbisdichlorobistriphenylphosphine (9.96 mg, 0.014 mmol), copper(I) iodide (1.351 mg, 7.09 μmol) and TEA (0.099 ml, 0.710 mmol) in THF (6 ml) was added (2R)-3-butyn-2-ol (24.85 mg, 0.355 mmol) and the reaction mixture was irradiated in a personal microwave reaction for 10 minutes at 120° C. The reaction mixture was diluted with EtOAc and washed with water. The solvent was removed and the crude material was purified via reverse phase HPLC to give 4-chloro-N-{[4-chloro-3-({3-chloro-5-[(3R)-3-hydroxy-1-butyn-1-yl]phenyl}oxy)-2-fluorophenyl]methyl}-1H-imidazole-5-carboxamide (16 mg, 0.033 mmol, 23% yield). 1H NMR (400 MHz, METHANOL-d4) δ ppm 7.24-7.45 (m, 3H), 7.11 (s, 1H), 6.89 (s, 1H), 6.74 (s, 1H), 4.47-4.70 (m, 3H), 1.41 (d, 3H). LC-MS (ES+) m/z 482.03, [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-ba6c4b2eea554c68ba4bebfacde85dc9 |
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| Source note | uspto-grants-2012_11 |
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