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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81770Generated: October 31, 2026

Water → 5-(5-Iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/81770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodine chlorideHCID 24640—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(4-Methoxy-2-(propan-2-yl)phenoxy)pyrimidine-2,4-diamineHCID 16117816—
SolventAcetic AcidHCID 176—
Product5-(5-Iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamineHCID 1595380293%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846705B2
Source datasetuspto-grants-2014_09
ORD IDord-14231d0ce4c64fd1a50bd02e2e01f6f7
Source noteuspto-grants-2014_09