Diisopropylethylamine → HCID 178489795, compound

HRID 16829

Reaction equation

HRID 16829 reaction equation
Cl[C:2]1[N:3]=[CH:4][C:5]([C:8]([NH:10][C:11]2[NH:12][N:13]=[C:14]([CH2:16][CH2:17][C:18]3[CH:23]=[C:22]([O:24][CH3:25])[CH:21]=[C:20]([O:26][CH3:27])[CH:19]=3)[CH:15]=2)=[O:9])=[N:6][CH:7]=1.[CH3:28][N:29]1[C@@H:34]([CH3:35])[CH2:33][NH:32][CH2:31][C@H:30]1[CH3:36].C[C@H]1CNC[C@@H](C)N1CC#N.C(N(C(C)C)C(C)C)C>CS(C)=O.CO>[CH3:27][O:26][C:20]1[CH:19]=[C:18]([CH2:17][CH2:16][C:14]2[CH:15]=[C:11]([NH:10][C:8]([C:5]3[CH:4]=[N:3][C:2]([N:32]4[CH2:33][C@H:34]([CH3:35])[N:29]([CH3:28])[C@H:30]([CH3:36])[CH2:31]4)=[CH:7][N:6]=3)=[O:9])[NH:12][N:13]=2)[CH:23]=[C:22]([O:24][CH3:25])[CH:21]=1

Participants

7

Reactant 4

HCID 81531DiisopropylethylamineHCID 30720221(2R,6S)-1,2,6-TrimethylpiperazineHCID 866210742-[(2S,6R)-2,6-dimethylpiperazin-1-yl]acetonitrileHCID 178489782HCID 178489782, compound

Product 1

HCID 178489795HCID 178489795, compoundYield 73%

Reagents, catalysts & solvents 2

HCID 679Dimethyl SulfoxideSolventHCID 887MethanolSolvent

Procedure

5-Chloro-N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]pyrazine-2-carboxamide (271 mg, 0.70 mmol) was added in one portion to a 3:1 mixture of (2R,6S)-1,2,6-trimethylpiperazine and 2-[(2S,6R)-2,6-dimethylpiperazin-1-yl]acetonitrile (180 mg, 1.40 mmol) in anhydrous dimethylsulfoxide (1.40 ml) at 25° C. The resulting solution was stirred at ambient temperature for 2 h. The reaction was incomplete and N-ethyl-N-propan-2-ylpropan-2-amine (0.24 ml, 1.40 mmol) was added and the solution was stirred at 60° C. for a further 2 h. The reaction mixture was diluted with methanol (20 mL) and purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH to afford impure material. The concentrated eluent was purified by silica column chromatography, eluting with a gradient of 0 to 5% 7M NH3/MeOH in DCM. Pure fractions were evaporated to dryness to afford the title compound (246 mg, 73%) as a yellow solid.

Workup

  1. stirringthe solution was stirred at 60° C. for a further 2 h
  2. custompurified by ion exchange chromatography
  3. washThe desired product was eluted from the column
  4. customto afford impure material
  5. customThe concentrated eluent was purified by silica column chromatography
  6. washeluting with a gradient of 0 to 5% 7M NH3/MeOH in DCM
  7. customPure fractions were evaporated to dryness

Sources & evidence

ORD record
ord-0519f2eedee94926bc73210350e77680
Source dataset
uspto-grants-2010_06
Patent number
US07737149B2

Linked notes

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