HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011924Generated: November 1, 2026
1-Chloro-3-iodobenzene → HCID 178463852, compound
https://huagongshe.com/reaction/1011924
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-3-iodobenzene | HCID 12269 | — |
| Reactant | (3-Diethylamino-pyrrolidin-1-yl)-[5-(3-ethynyl-phenyl)-4-methyl-1H-pyrazol-3-yl]-methanone | HCID 178436202 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | HCID 178463852 | HCID 178463852 | 65.1% |
Reaction Steps
A solution of 0.086 g (0.36 mmol) of 1-chloro-3-iodobenzene in 1.5 ml piperidine was degassed (argon) and treated with 17 mg (0.01 mmol) Pd(PPh3)4 and 3 mg (0.01 mmol) CuI. The reaction mixture was stirred at 50° C. for 10 min and then slowly (60 min) treated with 0.105 g (0.30 mmol) of (3-diethylamino-pyrrolidin-1-yl)-[5-(3-ethynyl-phenyl)-4-methyl-1H-pyrazol-3-yl]-methanone in 1.55 ml piperidine. After 30 min the bath was slowly (30 min) heated to 80° C. The reaction mixture was stirred at this temperature for 1 h and then partitioned between chilled water sat. KHCO3/Et2O (3×). The organic phases were washed with aqueous 10% NaCl, dried (Na2SO4) and evaporated. Purification by flash-chromatography on silica gel (CH2Cl2/MeOH 97.5:2.5 to 95:5) yielded 0.090 g (65%) of the title compound as light yellow foam. MS: 461.1 (MH+, 1 Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977358B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-c25c82e94ab14e96805c8fb67ae3fe09 |
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| Source note | uspto-grants-2011_07 |
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