Potassium Sodium Tartrate → N-((2-chloro-1-mesityl-6-(trifluoromethyl)-1H-imidazo[1,2-a]imidazol-5-yl)methyl)-N-(cyclopropylmethyl)propan-1-amine

HRID 1349430Notes

Reaction equation

HRID 1349430 reaction equation
[CH:1]1([CH2:4][N:5]([CH2:30][CH2:31][CH3:32])[C:6]([C:8]2[N:12]3[CH:13]=[C:14]([Cl:25])[N:15]([C:16]4[C:21]([CH3:22])=[CH:20][C:19]([CH3:23])=[CH:18][C:17]=4[CH3:24])[C:11]3=[N:10][C:9]=2[C:26]([F:29])([F:28])[F:27])=O)[CH2:3][CH2:2]1.COCCO[AlH2-]OCCOC.[Na+].[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+]>C1(C)C=CC=CC=1>[Cl:25][C:14]1[N:15]([C:16]2[C:17]([CH3:24])=[CH:18][C:19]([CH3:23])=[CH:20][C:21]=2[CH3:22])[C:11]2[N:12]([CH:13]=1)[C:8]([CH2:6][N:5]([CH2:4][CH:1]1[CH2:2][CH2:3]1)[CH2:30][CH2:31][CH3:32])=[C:9]([C:26]([F:27])([F:28])[F:29])[N:10]=2

Participants

5

Procedure

A solution of 6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[1,2-a]imidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide (27.2 mg, 0.058 mmol) in toluene (3 mL) was added a 65% solution of Red-Al in toluene (0.10 mL, 0.320 mmol). The reaction mixture was stirred at room temperature for 14 h. A solution of Rochelle's salt (2.0 mL) was added carefully at 0° C. and the mixture was vigorously stirred for 30 min. The crude product was extracted with ethyl acetate. The combined organic extracts were dried with Na2SO4. The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase preparative HPLC. Yield—12.8 mg (39%). LC/MS: tR=1.77 min., MS: [M+H]=453.

Workup

  1. stirringthe mixture was vigorously stirred for 30 min
  2. extractionThe crude product was extracted with ethyl acetate
  3. dry with materialThe combined organic extracts were dried with Na2SO4
  4. customThe solvent was removed under reduced pressure
  5. customthe crude product was purified by a reverse-phase preparative HPLC

Sources & evidence

ORD record
ord-9e5c6cbf2c584e73a8ec86d6cedff7a1
Source dataset
uspto-grants-2007_05
Patent number
US07211669B2

Reaction notes

Loading…