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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453408Generated: November 1, 2026

Methyl iodide → HCID 57526758, compound

https://huagongshe.com/reaction/1453408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMethylureaHCID 11719—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57526579HCID 57526579—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 57526758HCID 57526758—

Reaction Steps

Prepared from methyl 13-Cyclohexyl-3-(methyloxy)-6-((tetrahydro-2H-pyran-4-ylamino)carbonyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate by methylation using MeI and NaH in DMF in a similar manner as described before; Analytical thin layer chromatography (5% MeOH/CH2Cl2) Rf=0.50; Analytical HPLC method: Solvent A=10% MeOH-90% H2O-0.1% TFA, Solvent B=90% MeOH-10% H2O-0.1% TFA, Start % B=0, Final % B=100, Gradient time=2 min, Flow Rate=5 ml/min, Column: Xterra MS C18 S7 3.0×50 mm; LC/MS: (ES+) m/z (M+H)+=529.32, HPLC Rt=1.995 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473688B2
Source datasetuspto-grants-2009_01
ORD IDord-f7f1f3dc33964003aa3e251c504c482f
Source noteuspto-grants-2009_01