1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-cyclopropyl-5-(cyclopropylmethyl)-1-{4-[(ethylamino)carbonyl]phenyl}-1H-1,2,3-triazole-4-carboxamide

HRID 1717292Notes

Reaction equation

HRID 1717292 reaction equation
[CH:1]1([CH2:4][C:5]2[N:9]([C:10]3[CH:15]=[CH:14][C:13]([C:16]([NH:18][CH2:19][CH3:20])=[O:17])=[CH:12][CH:11]=3)[N:8]=[N:7][C:6]=2[C:21](O)=[O:22])[CH2:3][CH2:2]1.C1C=C[C:27]2N(O)N=[N:30][C:28]=2[CH:29]=1.C1(N)CC1.CCN=C=NCCCN(C)C>C(#N)C.CN(C=O)C>[CH:28]1([NH:30][C:21]([C:6]2[N:7]=[N:8][N:9]([C:10]3[CH:15]=[CH:14][C:13]([C:16]([NH:18][CH2:19][CH3:20])=[O:17])=[CH:12][CH:11]=3)[C:5]=2[CH2:4][CH:1]2[CH2:3][CH2:2]2)=[O:22])[CH2:29][CH2:27]1

Participants

6

Reactant 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 69828CyclopropylamineHCID 757711-HydroxybenzotriazoleHCID 685122045-(cyclopropylmethyl)-1-{4-[(ethylamino)carbonyl]phenyl}-1H-1,2,3-triazole-4-carboxylic acid

Product 1

HCID 57664870N-cyclopropyl-5-(cyclopropylmethyl)-1-{4-[(ethylamino)carbonyl]phenyl}-1H-1,2,3-triazole-4-carboxamideYield 183.8%

Reagents, catalysts & solvents 1

HCID 21891449acetonitrile N,N-dimethylformamideSolvent

Procedure

5-(Cyclopropylmethyl)-1-{4-[(ethylamino)carbonyl]phenyl}-1H-1,2,3-triazole-4-carboxylic acid (503 mg, 1.60 mmol) obtained in Example 96b), HOBt (109 mg, 0.800 mmol, 0.5 eq.) and cyclopropylamine (0.149 ml, 2.08 mmol, 1.3 eq.) were dissolved in acetonitrile-DMF (2:1, 8 ml), WSC (376 mg, 1.92 mmol, 1.2 eq.) was added, and the mixture was stirred at room temperature for 2.5 hr. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate (50 ml) and washed with 2% aqueous sodium carbonate solution (×2), 10% aqueous ammonium chloride solution and saturated brine. The aqueous layers were each extracted with ethyl acetate-hexane (3:1, 40 ml). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated, and diethyl ether was added to the residue. The precipitate was collected by filtration, washed with diethyl ether and dried to give the title compound as a white powder (518 mg, 1.47 mmol, 91.6%).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. additionthe residue was diluted with ethyl acetate (50 ml)
  3. washwashed with 2% aqueous sodium carbonate solution (×2), 10% aqueous ammonium chloride solution and saturated brine
  4. extractioneach extracted with ethyl acetate-hexane (3:1, 40 ml)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated
  7. additiondiethyl ether was added to the residue
  8. filtrationThe precipitate was collected by filtration
  9. washwashed with diethyl ether
  10. customdried

Sources & evidence

ORD record
ord-28ec4f5eb0c548f9a7cdabbbd4bd60e5
Source dataset
uspto-grants-2010_09
Patent number
US07803822B2

Reaction notes

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