HCID 68433360, compound → HCID 68430783, compound

HRID 1372459Notes

Reaction equation

HRID 1372459 reaction equation
[CH3:1][Mg]Br.[Br:4][C:5]1[CH:10]=[CH:9][C:8](/[CH:11]=[CH:12]/[C:13]([N:15]2[C@H:19]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:18][O:17][C:16]2=[O:26])=[O:14])=[CH:7][CH:6]=1>C1COCC1.CSC>[Br:4][C:5]1[CH:6]=[CH:7][C:8]([C@H:11]([CH3:1])[CH2:12][C:13]([N:15]2[C@H:19]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH2:18][O:17][C:16]2=[O:26])=[O:14])=[CH:9][CH:10]=1

Participants

5

Conditions

Temperature
-20 °C

Procedure

To a stirred solution of copper(II) bromide dimethylsulfide complex (8.78 g, 42.7 mmol) in THF (60 mL) and dimethylsulfide (30 mL) was added methylmagnesium bromide (12.7 mL, 3.0M in diethyl ether, 38.1 mmol) at −40° C. The resultant mixture was stirred at −40° C. for 30 min, then warmed to −20° C. The product from Step A (3.53 g, 9.48 mmol) in THF (30 mL) was added to the above reaction mixture over 1 h at −20° C. The resultant mixture was stirred at −20° C. for 2 h, then slowly warmed to room temperature and stirred at room temperature for 12 h. The reaction was quenched by slow addition of saturated aqueous ammonium chloride solution. The organic phase was separated and the aqueous phase was extracted with two portions of ethyl acetate. The combined organic layers were washed with saturated aqueous brine and concentrated in vacuo. Purification by flash chromatography (silica gel, 83:17 hexanes/ethyl acetate) afforded the desired product.

Workup

  1. temperatureslowly warmed to room temperature
  2. customThe reaction was quenched by slow addition of saturated aqueous ammonium chloride solution
  3. customThe organic phase was separated
  4. extractionthe aqueous phase was extracted with two portions of ethyl acetate
  5. washThe combined organic layers were washed with saturated aqueous brine
  6. concentrationconcentrated in vacuo
  7. customPurification by flash chromatography (silica gel, 83:17 hexanes/ethyl acetate)

Sources & evidence

ORD record
ord-520d8c6207044af791197b6eb97f3c0f
Source dataset
uspto-grants-2007_01
Patent number
US07157490B2

Reaction notes

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