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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588063Generated: October 31, 2026

Methyl iodide → HCID 178504026, compound

https://huagongshe.com/reaction/1588063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 19101102HCID 19101102—
SolventEthanolHCID 702—
ProductHCID 178504026HCID 17850402671.3%

Reaction Steps

Methyl iodide (1.05 g, 7.4 mmol) is added to an ethanol (50 mL) solution of N-[4,6-bis(1,1-dimethylethyl)-5-hydroxy-2-pyrimidinyl]thiourea (2.0 g, 7.1 mmol) and the mixture is heated at reflux under argon for 2.5 hours. The ethanol is evaporated under reduced pressure and the residue is taken up in 50 mL EtOAc. The EtOAc solution is washed with saturated NaHCO3 (3×50 mL) and 50 mL of brine. Drying over MgSO4 and evaporation of solvent gives an off-white solid. Recrystallization from ether/hexane gives 1.5 g (71%) of N-[4,6-bis(1,1-dimethylethyl)-5-hydroxy-2-pyrimidinyl]-S methyl isothiourea; mp 163°-165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05220025
Source datasetuspto-grants-1993_06
ORD IDord-3550b2d08311426e8583befc0e52e29f
Source noteuspto-grants-1993_06