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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769354Generated: November 3, 2026

Methyl iodide → Methyl 3-[N-methyl-3-(t-butylthio)-6-methoxyindol-2-yl]-2,2-dimethylpropanoate

https://huagongshe.com/reaction/1769354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexamethylphosphoramideHCID 12679—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl 3-[6-methoxy-3-(t-butylthio) indol-2-yl]-2,2-dimethylpropanoic acidHCID 54438884—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-[N-methyl-3-(t-butylthio)-6-methoxyindol-2-yl]-2,2-dimethylpropanoateHCID 18947604—

Reaction Steps

A solution of 1.75 g of the indole from Step A in 30 mL of THF and 3 mL HMPA was cooled to -78° C. and to this solution was slowly added a solution of 0.54M KHMDS in toluene (10.2 mL). The mixture was stirred at this temperature for 15 min. and treated with 0.34 mL of iodomethane. The mixture was stirred at -78° C. for 5 h, quenched with 1N HC1 (100 mL), extracted with ethyl acetate, and the organic layer washed with H2O, dried over Na2SO4 and evaporated to dryness. The residue was chromatographed on flash silica gel using ethyl acetate:hexane (20:80) as eluant to afford the title compound as a solid; m.p. 97-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380850
Source datasetuspto-grants-1995_01
ORD IDord-a1e55bf3467c44e49f35021a8b9ade97
Source noteuspto-grants-1995_01