Dimethyl Sulfate → HCID 73074217, compound

HRID 2042755Notes

Reaction equation

HRID 2042755 reaction equation
[C:1]([O:5][C:6]([N:8]([CH3:22])[CH:9]1[CH:13]([OH:14])[CH2:12][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].S(OC)(O[CH3:27])(=O)=O>C1COCC1>[C:1]([O:5][C:6]([N:8]([CH3:22])[CH:9]1[CH:13]([O:14][CH3:27])[CH2:12][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

4

Procedure

A suspension of Compound G (52 g, 0.16 mol) in THF (150 mL) was stirred at RT for about 30 min and cooled to −10 to −15° C. A solution of potassium hexamethyldisilylamide (KHMDS, 40 solution in THF, 144 mL, 0.256 mol) was slowly added while controlling the temperature between −5 and −15° C. After 15 min, dimethyl sulfate (18.7 mL, 1.20 mol) was added dropwise to the reaction mixture while maintaining a temperature between −10 and 0° C., and the resulting reaction mixture was then stirred at this temperature for about 30 min. The reaction mixture was quenched by the addition of water (100 mL), followed by acetic acid (50 mL). The product was extracted with methyl tert-butyl ether (2×150 mL). The combined organic layer was washed with water (100 mL), brine (50 mL) and dried over anhydrous Na2SO4. Evaporation under reduced pressure gave Compound H as an oil (54 g).

Workup

  1. temperaturecooled to −10 to −15° C
  2. customthe temperature between −5 and −15° C
  3. waitAfter 15 min
  4. temperaturewhile maintaining a temperature between −10 and 0° C.
  5. customthe resulting reaction mixture
  6. stirringwas then stirred at this temperature for about 30 min
  7. customThe reaction mixture was quenched by the addition of water (100 mL)
  8. extractionThe product was extracted with methyl tert-butyl ether (2×150 mL)
  9. washThe combined organic layer was washed with water (100 mL), brine (50 mL)
  10. dry with materialdried over anhydrous Na2SO4
  11. customEvaporation under reduced pressure

Sources & evidence

ORD record
ord-0aafb728f99045d6832b5fbfe4b07c11
Source dataset
uspto-grants-2013_11
Patent number
US08586601B2

Reaction notes

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