HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069716Generated: October 30, 2026
4-Pentyn-2-ol, (2S)- → HCID 178433232, compound
https://huagongshe.com/reaction/1069716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Pentyn-2-ol, (2S)- | HCID 7568329 | — |
| Reactant | HCID 178433242 | HCID 178433242 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178433232 | HCID 178433232 | — |
Reaction Steps
Using Method C above, (S)-pent-4-yn-2-ol (68 mg, 0.82 mmol) (see Example 81 below) was coupled with (Z)-1,3-dihydro-5-fluoro-4-iodo-3-[(4-methyl-1H-imidazol-5-yl)methylene]-2H-indol-2-one (100 mg, 0.27 mmol) (Starting Material 3 supra) using (Ph3P)4Pd (31 mg, 0.03 mmol) and Cul (6 mg) in a mixture of DMF (5 mL) and Et3N (5 mL) as solvent at 80° C. for 4 hrs. Upon completion, the reaction mixture was concentrated and the residue was chromatographed on a silica gel column with neat CH3CN then THF and finally MeOH as elution solvent. The resulting (S)-(Z)-1,3-Dihydro-5-fluoro-4-(4-hydroxy-1-pentynyl)-3-[(4-methyl-1H-imidazol-5-yl)methylene]-2H-indol-2-one was triturated with Et2O and then recrystalized from superheated EtOH. (Yield 57 mg, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06252086B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-f61c0d049a774d558accdd2f69040e0f |
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| Source note | uspto-grants-2001_06 |
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