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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541218Generated: November 1, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-(1-(3-Amino-4-methylbenzoyl)azepan-4-yl)benzonitrile

https://huagongshe.com/reaction/541218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-Amino-4-methylbenzoic acidHCID 75568—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Azepan-4-yl)benzonitrileHCID 68288907—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(1-(3-Amino-4-methylbenzoyl)azepan-4-yl)benzonitrileHCID 6828891575%

Reaction Steps

To a 4-mL vial was added 3-amino-4-methylbenzoic acid (27 mg, 0.18 mmol, 1.0 equiv), 4-(azepan-4-yl)benzonitrile (compound 40.4, 40 mg, 0.2 mmol, 1.1 equiv), hydroxybenzotriazole (39 mg of 20 wt % H2O, 0.23 mmol, 1.3 equiv), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (44 mg, 0.23 mmol, 1.3 equiv), DMF (1 mL) and N,N-diisopropylethylamine (93 μL, 0.54 mmol, 3.0 equiv). The mixture was stirred at room temperature for 4 hours then diluted into ethyl acetate (10 mL) and washed with brine (10 mL). The aqueous was extracted with ethyl acetate (3 mL) and the combined organics were washed with brine (10 mL), 1 M NaH2PO4 (5 mL) and brine (10 mL). The organics were dried (Na2SO4), filtered and concentrated to obtain the title compound as a brown solid (45 mg, 74%). m/z (ES+) 334 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-32b2a822a30f4affaec8519f8ecc72f2
Source noteuspto-grants-2014_10