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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885218Generated: November 1, 2026

Methyl iodide → HCID 178488069, compound

https://huagongshe.com/reaction/1885218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178488071HCID 178488071—
SolventMethanolHCID 887—
ProductHCID 178488069HCID 17848806991%

Reaction Steps

To a room temperature suspension of (Z)-5-[(5 -methoxy- 2-methyl-1H -indol -3-yl)methylene]-2-thioxo-4-thiazolidinone (1.714 g, 5.63 mmols) in 50 mL of methanol is added Hunig's base (1.15 mL, 6.61 mmols) followed by iodomethane (0.500 mL, 8.03 mmols). The thick suspension is stirred overnight at room temperature. Filtration washing with ether provides 1.631 g (91%) of (Z)-5-[(5-methoxy-2-methyl-1H-indol-3-yl)methylene]-2-(methylthio)-4-(5H)-thiazolone; mp 214°-222° C. dec. Calc'd for C15H14N2O2O2S2 :

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05143927
Source datasetuspto-grants-1992_09
ORD IDord-e6461d467e2b46439b58b8510245e906
Source noteuspto-grants-1992_09