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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865182Generated: October 31, 2026

Methyl iodide → HCID 11392341, compound

https://huagongshe.com/reaction/1865182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantHCID 11196840HCID 11196840—
SolventPyridineHCID 1049—
ProductHCID 11392341HCID 1139234120.3%

Reaction Steps

Add methyl iodide (20 mg, 0.164 mmol) at r.t. to a mixture of 3-phenylsulfanyl-1H-pyrrolo[3,2-b]pyridine-2-carboxylic acid methylamide (Ia-33, 47 mg, 0.166 mmol), Cs2CO3 (65 mg, 0.2 mmol) and pyridine (1.5 ml). Heat the reaction at 60° C. in a sealed vessel for 3 hrs. Add additional methyl iodide (20 mg) and monitor the progress on the reaction by chromatography. When complete, cool the mixture, concentrate to dryness and extract into ethyl acetate from brine. Separate the organic phase and concentrate. Purify the residue by flash chromatography twice (SiO2, 3 gm, elute with MeOH 0-4% in DCM; and SiO2, 1 gm, elute with heptane:DCM, 1:1) to provide title compound (10 mg) as a white solid, 1H NMR (CDCl3) and LC-MS (m/e=297) were consistent for the title compound structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626027B2
Source datasetuspto-grants-2009_12
ORD IDord-f419fe5df4db4dc09d9910a5caef8882
Source noteuspto-grants-2009_12