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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396474Generated: October 29, 2026

Hydrochloric Acid → HCID 19704898, compound

https://huagongshe.com/reaction/2396474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantLithium ChlorideHCID 433294—
Reactant1H-1-Benzazepine-2,5-dione, 3-methoxy-HCID 10750663—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19704898HCID 19704898—

Reaction Conditions

Temperature-70 °C

Reaction Steps

3-Methoxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepine (0.5 g) and anhydrous lithium chloride (0.63 g) were added to dry tetrahydrofuran (10 mL), and the mixture was cooled to -70° C. To this was added diisopropylamine (380 mL), followed by butyllithium (2.2 mL, 2.5 M in hexanes); and the mixture was warmed to -20° C. After 30 minutes, methyl iodide (307 mL) was added and the mixture cooled to -10° C. for 10 minutes. The mixture was diluted with water, acidified with 2 N hydrochloric acid and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried and evaporated. The solid was purified by chromatography, with ethyl acetate:toluene (1:1) as the eluent, and recrystallized from hot toluene to give the methylated product as a white solid (0.367 g); NHR: 2.03 (s,3); MS(EI): m/z=217(M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05492905
Source datasetuspto-grants-1996_02
ORD IDord-f2c0789e02274dc880e63c5a44c76e00
Source noteuspto-grants-1996_02