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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272561Generated: November 3, 2026

3-Amino-9-ethylcarbazole → N-(4-cyanophenyl)-5-[(9-ethyl-9H-carbazol-3-yl)amino]-3-methylpentanamide

https://huagongshe.com/reaction/2272561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-9-ethylcarbazoleHCID 8588—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(4-cyanophenyl)-3-methyl-5-oxopentanamideHCID 86729722—
SolventTolueneHCID 1140—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(4-cyanophenyl)-5-[(9-ethyl-9H-carbazol-3-yl)amino]-3-methylpentanamideHCID 8672972340.5%

Reaction Steps

A solution of the compound obtained in Step 2 (110 mg, 0.48 mmol) and 3-amino-N-ethylcarbazole (151 mg, 0.72 mmol) in TFA (1 mL) and toluene (1 mL) was stirred at room temperature for 1 hr. To the reaction mixture was added sodium triacetoxyborohydride (304 mg, 1.43 mmol), and the mixture was stirred at room temperature for additional 14 hr. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate. The solution was washed with 1N aqueous sodium hydroxide solution, water and saturated brine, and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 10 to 80% ethyl acetate/hexane) to give the title compound (82 mg, 0.193 mmol, 40.5%) as a pale-yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120776B2
Source datasetuspto-grants-2015_09
ORD IDord-53eecf6a4eb34ad48819c0ec56335949
Source noteuspto-grants-2015_09