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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565952Generated: October 29, 2026

Methyl iodide → HCID 18472360, compound

https://huagongshe.com/reaction/565952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18472660HCID 18472660—
SolventDichloromethaneHCID 6344—
ProductHCID 18472360HCID 18472360—

Reaction Steps

In dichloromethane (35ml) was dissolved N-(4(piperidin-2-ylcarbonyl)-phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (0.3g), and to the solution were added methyl iodide (0.08ml) and diisopropyl-ethylamine (0.17ml). The mixture was stirred at room temperature over night. The solvent was evaporated, and to the residue was added water. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column (ethyl acetate/methanol/triethylamine) to give crude crystals, which were recrystallized from ethyl acetate-hexane to give N-(4-(1-methylpiperidin-2-ylcarbonyl)-phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (Compound 157) (0.17g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-30f0ffa79a884848a7cf908bff77be1e
Source noteuspto-grants-2001_01