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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246192Generated: October 29, 2026

Methyl iodide → HCID 71285981, compound

https://huagongshe.com/reaction/246192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant18-Crown-6HCID 28557—
ReactantHCID 71286101HCID 71286101—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71285981HCID 7128598129%

Reaction Steps

In a 10 mL round-bottomed flask, 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-1-hydroxymethyl-3-methanesulfonyl-propyl)-amide (102 mg, 0.173 mmol) was dissolved in THF (1.9 ml) to give a colorless solution. The reaction was cooled in an ice bath and crushed KOH (97 mg, 1.73 mmol), 18-crown-6 (46 mg, 0.173 mmol), and iodomethane (11 μl, 0.173 mmol) were added successively. The reaction mixture was stirred at 0° C. for 1 h after which the ice bath was removed. The reaction mixture was stirred at room temperature for 2 h then diluted with dichloromethane (10 mL) and washed with aqueous ammonium chloride (10 mL), water (10 mL), and saturated sodium bicarbonate (10 mL). The organic layer was dried over Na2SO4 and concentrated. The crude material was purified by chromatography over SiO2 with EtOAc/heptane (gradient: 0%-60% EtOAc) to afford 30 mg (29%) of 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-1-methoxymethyl-3-methanesulfonyl-propyl)-amide as an off-white solid. MS: [M+Na]+=627).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-f84d92ec9f1c47cab0109905da144682
Source noteuspto-grants-2014_02