Sodium Methoxide → HCID 25121190, compound

HRID 2046382Notes

Reaction equation

HRID 2046382 reaction equation
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([N:14]([CH3:27])[C:15](=[O:26])[CH2:16][NH:17][C:18]2[C:23](Cl)=[CH:22][N:21]=[N:20][C:19]=2[Cl:25])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:28][O-:29].[Na+]>CO>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([N:14]([CH3:27])[C:15](=[O:26])[CH2:16][NH:17][C:18]2[C:23]([O:29][CH3:28])=[CH:22][N:21]=[N:20][C:19]=2[Cl:25])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 10942334Sodium MethoxideHCID 59336185HCID 59336185, compound

Product 1

HCID 25121190HCID 25121190, compoundYield 30.9%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A solution of Compound 139 (10 mg) and sodium methoxide (1.3 mg) in methanol (MIL) was stirred overnight under reflux. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by amino-coated silica gel (Fuji Sylysia Chemical Ltd.,; NH-DM1020) column chromatography (ethyl acetate:hexane=1:9 to 1:1) to give 3.0 mg (30% yield) of the desired product as a white amorphous.

Workup

  1. temperatureunder reflux
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customthe resulting residue was purified by amino-coated silica gel (Fuji Sylysia Chemical Ltd.,; NH-DM1020) column chromatography (ethyl acetate:hexane=1:9 to 1:1)

Sources & evidence

ORD record
ord-437628178eac4b1fac0180c81e98b446
Source dataset
uspto-grants-2013_11
Patent number
US08592435B2

Reaction notes

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