HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398551Generated: November 2, 2026
Sodium Iodide → 4-(6-Iodo-3-methylindazol-1-yl)pyrimidin-2-amine
https://huagongshe.com/reaction/1398551
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(6-bromo-3-methyl-1H-indazol-1-yl)pyrimidin-2-amine | HCID 68181865 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(6-Iodo-3-methylindazol-1-yl)pyrimidin-2-amine | HCID 68181636 | — |
Reaction Steps
A pressure tube containing copper (1) iodide (37.57 mg, 0.20 mmol), sodium iodide (591.42 mg, 3.95 mmol) and 4-(6-bromo-3-methyl-1H-indazol-1-yl)pyrimidin-2-amine (600 mg, 1.97 mmol) was flushed with nitrogen before the addition of 1,4-dioxane, DMF (3 ml each) and N,N′-dimethylethane-1,2-diamine (0.021 ml, 0.20 mmol). The vessel was sealed and stirred at 115° C. overnight. Reaction was cooled and added to ice water (15 ml) before extracting into DCM (2×20 mL). Combined organics were dried (Na2SO4), filtered and concentrated in vacuo. Crude material purified by column chromatography (Elution with 2% MeOH-DCM to 12% MeOH-DCM) to give the title compound: 1H NMR (500 MHz, DMSO) delta 7.02 (3H, dd, J=5.5, 3.1 Hz), 7.73-7.53 (2H, m), 8.25 (1H, d, J=5.5 Hz), 9.25 (1H, s); LC-MS: m/z=+351.90 (M+H)+. This compound of 79% purity LC-MS was used for the next step without further purification
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901313B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-f0bf8f10b68a41e3af1ed568c96c9348 |
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| Source note | uspto-grants-2014_12 |
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