Dimethylformamide → Ammonia

HRID 1946254Notes

Reaction equation

HRID 1946254 reaction equation
[CH3:1][O:2][C:3]1[C:17]([O:18][CH3:19])=[CH:16][C:6]2[NH:7][C:8]([C:10]3[C:14]([NH2:15])=[CH:13][NH:12][N:11]=3)=[N:9][C:5]=2[CH:4]=1.CN(C(ON1N=NC2C=[CH:32][CH:33]=[CH:34][C:29]1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[OH-:42].[Na+].[CH3:44][N:45]([CH:47]=O)[CH3:46]>>[NH3:7].[CH3:19][O:18][C:17]1[C:3]([O:2][CH3:1])=[CH:4][C:5]2[NH:9][C:8]([C:10]3[C:14]([NH:15][C:32]([CH:33]4[CH2:34][CH2:29][CH2:46][N:45]([CH3:44])[CH2:47]4)=[O:42])=[CH:13][NH:12][N:11]=3)=[N:7][C:6]=2[CH:16]=1

Participants

6

Procedure

To a solution of 3-(5,6-dimethoxy-1H-benzimidazol-2-yl)-1H-pyrazol-4-ylamine (65 mg, 0.25 mmol) (Example 15B) (rac)-1-methyl-piperidine-3-carboxylic acid-hydrocholoride salt (50 mg, 0.27 mmol) and disopropylethylamine (50 μl, 0.27 mmol) in DMF (1 ml) was added TBTU (97 mg, 0.30 mmol). The mixture was stirred at room temperature for approximately 16 hours after which 1N aqueous NaOH (1 ml) was added and the mixture stirred for a further 1 hours. The mixture was then evaporated to dryness in vacuo and the residue purified by flash column chromatography (SiO2, eluting with a gradient of DCM:MeOH (98:2) to DCM: MeOH; conc. Aq. NH3 (70:30:3) to give N-[3-(5,6-dimethoxy-1H-benzimidazol-2-yl)-1H-pyrazol-4-yl]-rac-1-methyl-piperidine 3-carboxamide (20 mg) as a colourless gum (LC/MS (basic method): Rt 2.35 min, (M+H)+ 385).

Workup

  1. additionwas added
  2. customThe mixture was then evaporated to dryness in vacuo
  3. customthe residue purified by flash column chromatography (SiO2
  4. washeluting with a gradient of DCM:MeOH (98:2) to DCM

Sources & evidence

ORD record
ord-d2bf815b03d2484a8e709584ef657998
Source dataset
uspto-grants-2013_03
Patent number
US08399442B2

Reaction notes

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