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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489087Generated: October 31, 2026

HCID 22903480, compound → HCID 22903475, compound

https://huagongshe.com/reaction/1489087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22903480HCID 22903480—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
ProductHCID 22903475HCID 2290347530.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 7-chloro-1-{6-[2-(2-methanesulfonyloxyethoxy)benzoylamino]nicotinoyl}-2,3,4,5-tetrahydro-1H-benzazepine (0.75 g) in dimethylformamide (10 ml) is added potassium phthalimide (0.26 g), and the mixture is stirred at 110° C. for one hour. The mixture is poured into ice-water, and extracted with dichloromethane. The extract is washed with water, dried over magnesium sulfate, and evaporated under reduced pressure. The residue is purified by silica gel column chromatography to give 7-chloro-1-[6-(6,7-benzo-1-oxo-4-azepin-5-on-4-yl)nicotinoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.23 g, Compound A) and 7-chloro-1-{6-[2-(2-phthalimidoethoxy)benzoylamino]nicotinoyl}-2,3,4,5-tetrahydro-1H-benzazepine (0.25 g, Compound B), separately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677299
Source datasetuspto-grants-1997_10
ORD IDord-80a208aa384241f5a5c4fb72e809084e
Source noteuspto-grants-1997_10