Diisopropylethylamine → (RS)-1-[2-(4,5-Difluoro-1H-benzoimidazol-2-ylmethyl)-piperidin-1-yl]-1-[5-(4-fluoro-phenyl)-2-methyl-thiazol-4-yl]-methanone

HRID 2077321Notes

Reaction equation

HRID 2077321 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]([CH3:13])=[N:10][C:9]=2[C:14]([OH:16])=O)=[CH:4][CH:3]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(CC)C(C)C)(C)C.[F:50][C:51]1[C:59]2[N:58]=[C:57]([CH2:60][CH:61]3[CH2:66][CH2:65][CH2:64][CH2:63][NH:62]3)[NH:56][C:55]=2[CH:54]=[CH:53][C:52]=1[F:67]>CN(C=O)C>[F:50][C:51]1[C:59]2[N:58]=[C:57]([CH2:60][CH:61]3[CH2:66][CH2:65][CH2:64][CH2:63][N:62]3[C:14]([C:9]3[N:10]=[C:11]([CH3:13])[S:12][C:8]=3[C:5]3[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=3)=[O:16])[NH:56][C:55]=2[CH:54]=[CH:53][C:52]=1[F:67]

Participants

6

Procedure

A solution of 5-(4-fluoro-phenyl)-2-methyl-thiazole-4-carboxylic acid (1.00 g, 4.2 mmol), HATU (1.60 g, 4.2 mmol) and N,N-diisopropylethylamine (2.00 ml, 11.6 mmol) in DMF (20 ml) was stirred at room temperature under argon for 2 min. The mixture was then treated with (RS)-4,5-difluoro-2-piperidin-2-ylmethyl-1H-benzoimidazole, D21 (1.06 g, 4.2 mmol) and stirring was continued for 16 h. The solvent was removed in vacuo and the residue was washed with water then was triturated with ethyl acetate to afford the title compound as an off-white solid (1.68 g, 85%).

Workup

  1. customThe solvent was removed in vacuo
  2. washthe residue was washed with water
  3. customthen was triturated with ethyl acetate

Sources & evidence

ORD record
ord-68bb4bcc76304d77b091f5f8a2264e67
Source dataset
uspto-grants-2011_04
Patent number
US07928124B2

Reaction notes

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