HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775510Generated: November 3, 2026
Iodine → N-(3-(2-chlorophenyl)-4-iodo-1-methyl-1H-pyrazol-5-yl)acetamide
https://huagongshe.com/reaction/1775510
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Iodic acid | HCID 24345 | — |
| Reactant | N-(3-(2-chlorophenyl)-1-methyl-1H-pyrazol-5-yl)acetamide | HCID 70983638 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-(2-chlorophenyl)-4-iodo-1-methyl-1H-pyrazol-5-yl)acetamide | HCID 70983478 | 379.8% |
Reaction Steps
To a solution of N-(3-(2-chlorophenyl)-1-methyl-1H-pyrazol-5-yl)acetamide (526 mg, 2.12 mmol) in ethanol (16 mL) were added iodic acid (93 mg, 0.53 mmol) and iodine (294 mg, 1.16 mmol). The reaction was stirred for 18 h at 50° C. The reaction mixture was concentrated in vacuo and the residue was dissolved in CH2Cl2 and washed with a 2 N Na2SO3 solution. The organic phase was dried over MgSO4, filtered and evaporated to give N-(3-(2-chlorophenyl)-4-iodo-1-methyl-1H-pyrazol-5-yl)acetamide as a light orange solid (756 mg), which was used as such in the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260381B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-fc042e7884f1438384d543ab080c0842 |
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| Source note | uspto-grants-2016_02 |
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