HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925157Generated: October 30, 2026
Water → 5-(5-Iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamine
https://huagongshe.com/reaction/925157
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(4-Methoxy-2-(propan-2-yl)phenoxy)pyrimidine-2,4-diamine | HCID 16117816 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(5-Iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamine | HCID 15953802 | 93% |
Reaction Steps
To a solution of 5-(2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine (0.40 g, 1.44 mmol) in glacial acetic acid (4 ml) at room temperature was added a solution of iodine monochloride (0.28 g, 1.76 mmol) in glacial acetic acid (4 ml). Water (6 ml) was also added, and the reaction was stirred for 16 hours, after which another portion of iodine monochloride (0.4 g, 2.47 mmol) in glacial acetic acid (4 ml) was added. The reaction mixture was stirred for an additional hour at room temperature. The acidic mixture was basified with saturated NaHCO3 solution and extracted into dichloromethane. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography (5% CH3OH in CH2CL2 with 0.1% NH4OH) to give 5-(5-iodo-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine as beige colored solid (0.536 g, 92%). M+H 400.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284279B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-93052dbe66cc4bb9ab703dc84a5200ad |
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| Source note | uspto-grants-2016_03 |
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