Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839401Generated: November 1, 2026

Methyl iodide → HCID 21948140, compound

https://huagongshe.com/reaction/1839401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 21948182HCID 21948182—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 21948140HCID 21948140—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a suspension of 2,2,6,6-tetramethylpiperidine (153 mg, 0.18 mL, 1.08 mmol) in THF (10 mL) at 0° C., was added n-BuLi via syringe (1.6 M, 0.68 mL, 1.08 mmol) and TMEDA. The reaction mixture was stirred for 1 h under argon. The reaction mixture was cooled to −60° C. using an acetone/dry ice bath and 2-anilino-7-ethoxy-5-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (100 mg, 0.269 mmol) was added via syringe as a solution in THF (5 mL). The mixture was stirred for 1 h. MeI was added via syringe and the reaction was allowed to warm to room temperature and stirred for 18 h. A saturated aqueous solution of NH4Cl (20 mL) and EtOAc (20 mL) was added, and the organic layer was separated, dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel flash chromatography using 7:3 to 100:0 EtOAc:Hex to give 3 products as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677352B1
Source datasetuspto-grants-2004_01
ORD IDord-7aad9a83a649412285930e2d12c22225
Source noteuspto-grants-2004_01