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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445176Generated: October 30, 2026

Methyl iodide → HCID 60112881, compound

https://huagongshe.com/reaction/445176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexamethylphosphoramideHCID 12679—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 10210971HCID 10210971—
ProductHCID 60112881HCID 60112881—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1.20 g (2 mmol) of N-{3-[4-(4-isopropyl-phenyl)-2-oxo-6-propargyloxy-2H-quinazolin-1-ylmethyl]-phenyl}-2-[4-(2-methoxy-ethyl)-piperazin-1-yl]-acetamide is treated with 4.1 ml 0.5 M LDA-solution (in THF) and 0.35 ml (2.0 mmol) HMPT at −78° C. The cooling bath is removed and stirring continued for half an hour while the solution turns slowly red. The reaction mixture is cooled down again to −78° C., 284 μl methyl iodide (2 mmol; diluted with 5 ml THF) is added. After stirring overnight at rt, the orange solution is concentrated in vacuo The yellow foamy residue is purified by chromatography (CH2Cl2/MeOH 9:1). Yield: 480 mg (13%) yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476286B2
Source datasetuspto-grants-2013_07
ORD IDord-14a3eecf07994c378ba0e72d5ea97594
Source noteuspto-grants-2013_07