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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272578Generated: November 3, 2026

Diisopropylethylamine → N-(4-cyanophenyl)-3-methyl-N'-[9-(2-methylpropyl)-2,3,4,9-tetrahydro-1H-carbazol-6-yl]pentanediamide

https://huagongshe.com/reaction/2272578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 3981627HCID 3981627—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant9-isobutyl-2,3,4,9-tetrahydro-1H-carbazol-6-amineHCID 86729736—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(4-cyanophenyl)-3-methyl-N'-[9-(2-methylpropyl)-2,3,4,9-tetrahydro-1H-carbazol-6-yl]pentanediamideHCID 8672973753.1%

Reaction Steps

To a solution of the compound obtained in Step 2 (235 mg, 0.97 mmol), 5-(4-cyanophenylamino)-3-methyl-5-oxopentanoic acid (239 mg, 0.97 mmol) and DIEA (0.508 mL, 2.91 mmol) in DMF (6 mL) was added HATU (553 mg, 1.45 mmol), and the mixture was stirred at room temperature for 14 hr. To the reaction solution was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with 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; 5 to 75% ethyl acetate/hexane) to give the title compound (242 mg, 0.515 mmol, 53.1%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120776B2
Source datasetuspto-grants-2015_09
ORD IDord-ce24647ba16446d6857f46401542d9c7
Source noteuspto-grants-2015_09