Water → 1-[4-(4-Fluoro-phenyl)-1-methyl-1H-pyrazol-3-yl]-1-((S)-2-{[5-(1-hydroxy-ethyl)-pyrimidin-2-ylamino]-methyl}-piperidin-1-yl)-methanone

HRID 18107Notes

Reaction equation

HRID 18107 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:14]([N:16]3[CH2:21][CH2:20][CH2:19][CH2:18][C@H:17]3[CH2:22][NH:23][C:24]3[N:29]=[CH:28][C:27]([C:30](=[O:32])[CH3:31])=[CH:26][N:25]=3)=[O:15])=[N:10][N:11]([CH3:13])[CH:12]=2)=[CH:4][CH:3]=1.[BH4-].[Na+].O>CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:9]([C:14]([N:16]3[CH2:21][CH2:20][CH2:19][CH2:18][C@H:17]3[CH2:22][NH:23][C:24]3[N:25]=[CH:26][C:27]([CH:30]([OH:32])[CH3:31])=[CH:28][N:29]=3)=[O:15])=[N:10][N:11]([CH3:13])[CH:12]=2)=[CH:6][CH:7]=1

Participants

5

Procedure

1-{2-[((S)-1-{1-[4-(4-Fluoro-phenyl)-1-methyl-1H-pyrazol-3-yl]-methanoyl}-piperidin-2-ylmethyl)-amino]-pyrimidin-5-yl}-ethanone (0.2 g) was dissolved in methanol 20 ml) and sodium borohydride (0.4 g) added. The reaction was stirred overnight, water was added and stirring continued for 30 min. The reaction mixture was extracted with ethyl acetate (x3), the organic extracts combined, dried (MgSO4) and solvent removed at reduced pressure to give the title compound as a colourless foam.

Workup

  1. additionadded
  2. stirringstirring
  3. waitcontinued for 30 min
  4. extractionThe reaction mixture was extracted with ethyl acetate (x3)
  5. dry with materialdried (MgSO4) and solvent
  6. customremoved at reduced pressure

Sources & evidence

ORD record
ord-5050cd275b4c48fd9ee56a3f15b226fc
Source dataset
uspto-grants-2010_06
Patent number
US07741329B2

Reaction notes

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