Diisopropylethylamine → HCID 68421046, compound

HRID 1765059Notes

Reaction equation

HRID 1765059 reaction equation
[CH2:1]([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[N:16]=[CH:15][N:14]([C:17]3[CH:22]=[CH:21][N:20]=[C:19](Cl)[CH:18]=3)[N:13]=2)=[CH:7][CH:6]=1)[CH3:2].[CH3:25][C@H:26]1[NH:31][C@@H:30]([CH3:32])[CH2:29][NH:28][CH2:27]1.CCN(C(C)C)C(C)C.[CH3:42][C:43](OCC1C2C(=CC=CC=2)C(COC(C)=O)=C2C=1C=CC=C2)=[O:44]>CN1C(=O)CCC1.C(Cl)Cl.CN(C=O)C>[CH2:1]([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[N:16]=[CH:15][N:14]([C:17]3[CH:22]=[CH:21][N:20]=[C:19]([N:28]4[CH2:29][CH:30]([CH3:32])[N:31]([C:43](=[O:44])[CH3:42])[CH:26]([CH3:25])[CH2:27]4)[CH:18]=3)[N:13]=2)=[CH:7][CH:6]=1)[CH3:2]

Participants

8

Reactant 4

HCID 81531DiisopropylethylamineHCID 613145Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 6950261rel-(2R,6S)-2,6-dimethylpiperazineHCID 58883268HCID 58883268, compound

Product 1

HCID 68421046HCID 68421046, compoundYield 44%

Reagents, catalysts & solvents 3

HCID 6228DimethylformamideSolventHCID 6344DichloromethaneSolventHCID 13387N-methyl-2-pyrrolidoneSolvent

Conditions

Temperature
250 °C

Procedure

To a solution of 500 mg of 4-[1-(2-Chloro-pyridin-4-yl)-1H-[1,2,4]triazol-3-ylamino]-benzoic acid ethyl ester (1.45 mMol, 1 equiv) in 10 mL of NMP was added 400 mg of cis—3,5 dimethyl piperazine (3.50 mMol, 2.41 equiv). The stirred solution was heated to 250° C. via microwave irradiation for 15 min. The crude product was precipitated by pouring into 100 mL of water and isolated by filtration. The crude product was then redissolved in 10 mL of CH2Cl2 and 2 mL of DMF. To the stirred solution was added sequentially 1 mL of Hunig's base and 500 μL of acetic anhydridide. After 3 hr at 25° C., the reaction mixture was concentrated to a dark oil and purifed by flash chromatography (10:1 CH.2Cl2:MeOH), yielding 300 mg of 4-{1-[2-(4-Acetyl-3,5-dimethyl-piperazin-1-yl)-pyridin-4-yl]-1H-[1,2,4]triazol-3-ylamino}-benzoic acid ethyl ester (0.647 mMol, 44% yield) as a white solid. 1H NMR (500 MHz, CDCl3) ∂ 8.44 (1H, s), 8.22 (1H, d), 8.05 (2H, d), 7.61 (3H, m), 7.27 (1H, s), 7.02 (1H, s), 6.86 (1H, d), 4.40 (2H, q), 3.50 (2H, q), 3.40 (2H, m), 3.20 (2H, m), 2.20 (3H, s), 1.40 (6H, m), 1.20 (3H, t) ppm. LC/MS: 2.68 min/464 (M+1).

Workup

  1. customThe crude product was precipitated
  2. additionby pouring into 100 mL of water
  3. customisolated by filtration
  4. concentrationthe reaction mixture was concentrated to a dark oil

Sources & evidence

ORD record
ord-a80b354d2b3d4632847fef8bb71c1e78
Source dataset
uspto-grants-2007_06
Patent number
US07226920B2

Reaction notes

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