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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893906Generated: October 31, 2026

Iodine → HCID 57606984, compound

https://huagongshe.com/reaction/1893906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 5243908HCID 5243908—
SolventMethanolHCID 887—
ProductHCID 57606984HCID 5760698485%

Reaction Steps

Iodine (3.04 g, 12.0 mmol) was added to a solution of N4-benzyl-6-methylpyrimidine-2,4-diamine (2.33 g, 10.9 mmol) in anhydrous MeOH (50 mL) at 0° C. The reaction was allowed to warm to room temperature overnight. After 12 hours, an additional 0.5 equiv of iodine was added, and the reaction warmed to 50° C. After four hours, the reaction was cooled to room temperature and concentrated in vacuo. The residue was diluted with ethyl acetate (200 mL) and washed with 10% NaHSO3 (200 mL). The aqueous phase was separated and washed once more with ethyl acetate (200 mL). The organic phases were combined, washed with brine, separated and dried over Na2SO4, The filtrate was concentrated in vacuo to afford the product N4-benzyl-5-iodo-6-methylpyrimidine-2,4-diamine (3.14 g, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513266B2
Source datasetuspto-grants-2013_08
ORD IDord-50fa307761c34ab28229a0bad44572ed
Source noteuspto-grants-2013_08