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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394894Generated: November 2, 2026

7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide → 5H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide

https://huagongshe.com/reaction/1394894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamideHCID 68846942—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamideHCID 68849291—

Reaction Steps

10% Palladium on carbon (70 mg, 0.07 mmol) was added to a solution of 7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide, 13-cyclohexyl-N10-[(dimethylamino)sulfonyl]-N6-(2-hydroxyethyl)-3-methoxy-N6-methyl- (64 mg, 0.11 mmol) in MeOH (3 mL) and the reaction mixture was vacuum flushed with nitrogen (3×) and then with hydrogen (3×). The reaction was stirred under a balloon of hydrogen overnight, filtered through a pad of celite and concentrated to yield 5H-indolo[2,1-a][2]benzazepine-6,10-dicarboxamide, 13-cyclohexyl-N10-[(dimethylamino)sulfonyl]-6,7-dihydro-N6-(2-hydroxyethyl)-3-methoxy-N6-methyl-(50 mg, 0.08 mmol, 78%) as a yellow solid. Mixture of atrope diasteromers:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348425B2
Source datasetuspto-grants-2008_03
ORD IDord-31163c0607e44434b0babd5b1c9f6394
Source noteuspto-grants-2008_03