Dimethylformamide → HCID 86642144, compound

HRID 2201960Notes

Reaction equation

HRID 2201960 reaction equation
C([Li])CCC.[C:6]([Si:10]([CH3:38])([CH3:37])[O:11][C@H:12]([C:18]1[CH:23]=[CH:22][C:21]([C:24]2[C@@H:28]([CH2:29][CH2:30][CH2:31][C:32]3[S:33][CH:34]=[CH:35][CH:36]=3)[CH2:27][CH2:26][CH:25]=2)=[CH:20][CH:19]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])([CH3:9])([CH3:8])[CH3:7].CN([CH:42]=[O:43])C>CCOCC>[C:6]([Si:10]([CH3:38])([CH3:37])[O:11][C@H:12]([C:18]1[CH:19]=[CH:20][C:21]([C:24]2[C@@H:28]([CH2:29][CH2:30][CH2:31][C:32]3[S:33][C:34]([CH:42]=[O:43])=[CH:35][CH:36]=3)[CH2:27][CH2:26][CH:25]=2)=[CH:22][CH:23]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])([CH3:9])([CH3:7])[CH3:8]

Participants

5

Procedure

n-Butyllithium (0.14 mL, 0.22 mmol, 1.6 M/hexanes) was added to an ice cold solution of 41 (53 mg, 0.11 mmol) in 0.5 mL ether. After 1 h, DMF (85 μL, 1.1 mmol) was added and the reaction was allowed to stir for 40 min. At this time, the reaction was quenched by addition of 10 mL saturated NH4Cl solution. The mixture was extracted with ethyl acetate (2×20 mL) and the combined ethyl acetate solution was dried (Na2SO4), filtered and evaporated. The residue was purified by flash chromatography using a Combiflash unit by Teledyne Isco (12 g silica gel, 0%→15% ethyl acetate/hexanes) which gave the title compound (43 mg, 0.084 mmol, 77%).

Workup

  1. customAt this time, the reaction was quenched by addition of 10 mL saturated NH4Cl solution
  2. extractionThe mixture was extracted with ethyl acetate (2×20 mL)
  3. dry with materialthe combined ethyl acetate solution was dried (Na2SO4)
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue was purified by flash chromatography

Sources & evidence

ORD record
ord-34f642c8ea624cc599bba21936579494
Source dataset
uspto-grants-2016_06
Patent number
US09365485B2

Reaction notes

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