Methanol → HCID 25128918, compound

HRID 587944Notes

Reaction equation

HRID 587944 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:32]=[CH:33][C:34]=1[O:35][CH3:36])[CH2:6][CH2:7][N:8]([CH3:31])[CH2:9][CH2:10][CH2:11][C:12]([C:21]1[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[C:23]([O:29][CH3:30])[CH:22]=1)(C(OC)=O)[C:13]([O:15][CH3:16])=[O:14].CO.[H-].[Na+]>C1COCC1.C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:32]=[CH:33][C:34]=1[O:35][CH3:36])[CH2:6][CH2:7][N:8]([CH3:31])[CH2:9][CH2:10][CH2:11][CH:12]([C:21]1[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[C:23]([O:29][CH3:30])[CH:22]=1)[C:13]([O:15][CH3:16])=[O:14]

Participants

6

Conditions

Temperature
22 °C

Procedure

To a solution of 0.349 g (0.694 mmol) of 3a in 20 mL of THF at 22° C. was added 0.281 mL (6.94 mmol) of methanol followed by 56 mg (1.39 mmol) of NaH (60% dispersion in mineral oil). The reaction was refluxed for 1 h, cooled to 22° C. and diluted with 100 mL of DCM. The mixture was washed with 50 mL of saturated NaHCO3, 50 mL of water, dried, and evaporated to give an oil. The oil was purified by flash chromatography on silica gel, eluting first with 2% methanol/DCM and then gradually increasing to 4% methanol/DCM to give 3b as a colorless oil; MS found M+H=446. The oxalate salt of 3r was recrystallized from ethyl acetate; mp 112-113.5° C.

Workup

  1. temperatureThe reaction was refluxed for 1 h
  2. washThe mixture was washed with 50 mL of saturated NaHCO3, 50 mL of water
  3. customdried
  4. customevaporated
  5. customto give an oil
  6. customThe oil was purified by flash chromatography on silica gel
  7. washeluting first with 2% methanol/DCM
  8. temperaturegradually increasing to 4% methanol/DCM

Sources & evidence

ORD record
ord-6635e1b95ff04b5496d9222a5ebb4e2b
Source dataset
uspto-grants-2016_01
Patent number
US09227918B2

Reaction notes

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