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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479499Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-methyl-N-[2,2,2-trichloro-1-[(Z)-[(cyanoamino)-(pyridin-3-ylamino)methylidene]amino]ethyl]benzamide

https://huagongshe.com/reaction/479499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(1-amino-2,2,2-trichloroethyl)-4-methylbenzamideHCID 18770673—
ReactantN-cyano-N'-(3-pyridinyl)thioureaHCID 18770764—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-methyl-N-[2,2,2-trichloro-1-[(Z)-[(cyanoamino)-(pyridin-3-ylamino)methylidene]amino]ethyl]benzamideHCID 17842586936.8%

Reaction Steps

A solution of Example 44A (200 mg, 0.932 mmol) in DMF (7 mL) at 23° C. was treated with EDCI (250 mg, 1.30 mmol) followed by diisopropyethylamine (0.180 mL, 1.03 mmol). The mixture was stirred for 30 minutes, then treated with a solution of Example 38A (262 mg, 0.932 mmol) as a solution in DMF (2 mL) along with additonal diisopropyethylamine (0.360 mL, 2.06 mmol). The solution was stirred for 10 hours, poured into ethyl acetate (25 mL), and washed with water (25 mL). The aqueous layer was extracted with ethyl acetate (20 mL), and the combined organic portions were washed with water (3×20 mL) and brine (20 mL). The organic portion was dried (Na2SO4), filtered, and concentrated. Purification of the residue by flash chromatography (elution with 5% ethanol/hexanes) provided 146 mg of the desired product as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645968B2
Source datasetuspto-grants-2003_11
ORD IDord-0db2a288bafc43e3ab55640b0c826992
Source noteuspto-grants-2003_11