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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(1-amino-2,2,2-trichloroethyl)-4-methylbenzamide | HCID 18770673 | — |
| Reactant | N-cyano-N'-(3-pyridinyl)thiourea | HCID 18770764 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-methyl-N-[2,2,2-trichloro-1-[(Z)-[(cyanoamino)-(pyridin-3-ylamino)methylidene]amino]ethyl]benzamide | HCID 178425869 | 36.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645968B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-0db2a288bafc43e3ab55640b0c826992 |
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| Source note | uspto-grants-2003_11 |
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