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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880004Generated: October 30, 2026

Hydrochloric Acid → 7-(4-(methyloxy)-2-{[(4-methyl-2-pyridinyl)methyl]oxy}phenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/880004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-dimethylethyl 7-(4-(methyloxy)-2-{[(4-methyl-2-pyridinyl)methyl]oxy}phenyl)-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylateHCID 70665023—
Solvent1,4-DioxaneHCID 31275—
Product7-(4-(methyloxy)-2-{[(4-methyl-2-pyridinyl)methyl]oxy}phenyl)-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 70665241—

Reaction Steps

1,1-dimethylethyl 7-(4-(methyloxy)-2-{[(4-methyl-2-pyridinyl)methyl]oxy}phenyl)-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate (4.8 g) was dissolved in dioxane (20 ml). Gaseous hydrogen chloride was passed through the reaction mixture for 1.5 h. The reaction was monitored by TLC. On completion the solid formed was collected by filtration and washed with acetone. The solid was then dissolved in water and the mixture was brought to pH8 using aqueous sodium bicarbonate. The sticky solid observed was extracted with DCM. The organics were dried over sodium sulphate and concentrated in vacuo to yield a solid. This was purified by column chromatography eluting with 0-8% methanol in DCM. Appropriate fractions were combined and concentrated in vacuo to yield a solid. This was triturated in diethyl ether to yield the title compound, 1.7 g (45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993560B2
Source datasetuspto-grants-2015_03
ORD IDord-d2c9c545e07b4da39e27f05ce453c8d1
Source noteuspto-grants-2015_03