Methanol → HCID 66672865, compound

HRID 1269399Notes

Reaction equation

HRID 1269399 reaction equation
[CH3:1][C@@:2]1([CH2:8][CH2:9][C:10]2[N:11]([CH3:27])[CH:12]=[C:13]([C:15](=[O:26])[CH2:16][CH2:17][CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH:14]=2)[CH2:6][O:5]C(=O)[NH:3]1.O1CCCC1.CO.[OH-].[K+]>O>[NH2:3][C@:2]([CH3:1])([CH2:8][CH2:9][C:10]1[N:11]([CH3:27])[CH:12]=[C:13]([C:15](=[O:26])[CH2:16][CH2:17][CH2:18][CH2:19][C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:14]=1)[CH2:6][OH:5]

Participants

6

Reactant 4

HCID 887MethanolHCID 8028TetrahydrofuranHCID 14797Potassium HydroxideHCID 66673133HCID 66673133, compound

Product 1

HCID 66672865HCID 66672865, compoundYield 87.6%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a solution of (4R)-4-methyl-4-{2-[1-methyl-4-(5-phenylpentanoyl)pyrrol-2-yl]ethyl}-1,3-oxazolidin-2-one (11 mg, 0.03 mmol) obtained in Example (38a) in a mixed solvent of tetrahydrofuran (1 ml) and methanol (1 ml) was added a 5N aqueous potassium hydroxide solution (1 ml), and the resulting mixture was refluxed for 2 days. After cooling, water was added to the reaction mixture, and the resulting mixture was extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate. After filtration, the solvent was removed in vacuo to afford the crude product of (2R)-2-amino-2-methyl-4-[1-methyl-4-(5-phenylpentanoyl)pyrrol-2-yl]butan-1-ol (9 mg).

Workup

  1. temperaturethe resulting mixture was refluxed for 2 days
  2. temperatureAfter cooling
  3. extractionthe resulting mixture was extracted with dichloromethane
  4. dry with materialThe extract was dried over anhydrous sodium sulfate
  5. filtrationAfter filtration
  6. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-e735ed59a8464233aa5a0460dff68cc8
Source dataset
uspto-grants-2007_04
Patent number
US07199150B2

Reaction notes

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