Water → HCID 59688513, compound

HRID 1593280Notes

Reaction equation

HRID 1593280 reaction equation
[OH:1][CH2:2][C@@H:3]([N:10]([CH3:22])[C:11]([CH:13]1[CH:15]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[O:14]1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Mg+2].[I-].[I-].[Cl-].[NH4+].O>C1(C)C=CC=CC=1>[OH:14][C@@H:13]1[C@@H:15]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[O:1][CH2:2][C@@H:3]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)[N:10]([CH3:22])[C:11]1=[O:12]

Participants

6

Procedure

To a stirred solution of (2RS,3RS)—N-[(1S)-2-hydroxy-1-phenylethyl]-N-methyl-3-phenyloxirane-2-carboxamide (30a) (1.7 g, 5.72 mmol) in anhydrous toluene (120 mL) was added MgI2 (1.6 g, 5.72 mmol, 98% purity) and the mixture vigorously stirred at RT for 32 h. The mixture was treated with saturated ammonium chloride (50 mL) and water (50 mL) and stirred for 30 min. The separated organic layer was washed consecutively with saturated ammonium chloride and brine, dried, filtered and evaporated to an orange oil (1.6 g). Isocratic flash column chromatography (2:1 hexanes-ethyl acetate) separated the title compound (33b) (400 mg, 24%) as a white solid from the (3S,6S,7R) diastereomer (1.0 g, 59%). There was a significant NOE observed between proton 3 and proton 7. HPLC: 1.78 min (Method A).

Workup

  1. stirringstirred for 30 min
  2. washThe separated organic layer was washed consecutively with saturated ammonium chloride and brine
  3. customdried
  4. filtrationfiltered
  5. customevaporated to an orange oil (1.6 g)
  6. customIsocratic flash column chromatography (2:1 hexanes-ethyl acetate) separated the title compound (33b) (400 mg, 24%) as a white solid from the (3S,6S,7R) diastereomer (1.0 g, 59%)
  7. custom1.78 min (Method A)

Sources & evidence

ORD record
ord-6efce2ccb08d4ad49575bdfe89c7621f
Source dataset
uspto-grants-2007_11
Patent number
US07294622B2

Reaction notes

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