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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658410Generated: November 1, 2026

Trimethylsilyldiazomethane → HCID 178504168, compound

https://huagongshe.com/reaction/658410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 59026796HCID 59026796—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 178504168HCID 17850416840%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of TMSdiazomethane (2 M, 90 μL, 0.18 mmol) in ether (2 mL) at 0° C., was added butyl lithium (2.5 M, 72 μL, 0.18 mmol) dropwise. The mixture was stirred for 20 min at 0° C. 3-[(2-fluoro-4-iodophenyl)amino]isonicotinonitrile (50 mg, 0.15 mmol) was then added into the solution. The reaction was allowed to warm to room temperature and proceed for three days. The mixture was diluted with ether and washed with saturated ammonium chloride solution, water, and dried over solid Na2SO4. The organic phase was concentrated, and the resulting residue was applied to chromatography in silica gel to give the desired product in 40% yield (27 mg). LC/MS [Method A: rt: 0.40 min; m/z: 454 (M+1)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076486B2
Source datasetuspto-grants-2011_12
ORD IDord-bee8378ba01f4c0ba0353243750e2bba
Source noteuspto-grants-2011_12