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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415665Generated: November 1, 2026

Methyl iodide → HCID 474633, compound

https://huagongshe.com/reaction/1415665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 474631HCID 474631—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 474633HCID 474633—

Reaction Steps

To a solution of 5,11-dihydro-11-ethyl-5-methyldipyrido[3,2-b:2',3'-e]azepine-6-one (0.10 g) in DMSO (1 mL) stirred under nitrogen was added potassium tert-butoxide (1M in tetrahydrofuran, 0.5 mL). After 3 minutes, methyl iodide (0.1 mL) was added, and the mixture was stirred for 10 minutes. Ethyl acetate was added, and the mixture was washed with water, dried, filtered, and evaporated. The residue was fractionated by preparative layer chromatography (developer chloroform/ethanol) to give 5,11-dihydro-11-ethyl-11-methyl-5-methyldipyrido[3,2-b:2',3 '-e]azepine-6-one (0.006 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908841
Source datasetuspto-grants-1999_06
ORD IDord-afc6b8e24d0b46c89c6e423226f95db1
Source noteuspto-grants-1999_06