HCID 59749551, compound → HCID 68773320, compound

HRID 747266Notes

Reaction equation

HRID 747266 reaction equation
[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([C:11]([C:13]3[N:14]=[CH:15][N:16]([C:18]([C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)([C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=4)[C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)[CH:17]=3)=[O:12])[C:5]=2[O:4][CH2:3][CH2:2]1.[CH3:37][Mg+].[Br-]>C1COCC1.CCOCC>[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([C:11]([C:13]3[N:14]=[CH:15][N:16]([C:18]([C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)([C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)[C:25]4[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=4)[CH:17]=3)([OH:12])[CH3:37])[C:5]=2[O:4][CH2:3][CH2:2]1

Participants

5

Procedure

A solution of (2,3-dihydro-benzo[1,4]dioxin-5-yl)-(1-trityl-1H-imidazol-4-yl)-methanone (Intermediate B1) (0.91 g, 1.93 mmol) in THF (80 mL) at −10° C. was treated with MeMgBr (2.6 mL, 7.68 mmol of a 3M solution in Et2O) for 45 m. The mixture was quenched with a sat. solution of NH4Cl and water. The layers were separated and the organic layer dried over MgSO4. The suspension was filtered and evaporated to dryness. The material was purified by chromatography on SiO2 with 50% EtOAc in CHCl3 to give 1-(2,3-dihydro-benzo[1,4]dioxin-5-yl)-1-(1-trityl-1H-imidazol-4-yl)-ethanol as a foam 0.95 g (98%).

Workup

  1. customThe mixture was quenched with a sat. solution of NH4Cl and water
  2. customThe layers were separated
  3. dry with materialthe organic layer dried over MgSO4
  4. filtrationThe suspension was filtered
  5. customevaporated to dryness
  6. customThe material was purified by chromatography on SiO2 with 50% EtOAc in CHCl3

Sources & evidence

ORD record
ord-b43316dc28064edd95bfc0153ba4fe2a
Source dataset
uspto-grants-2008_07
Patent number
US07396849B2

Reaction notes

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