Serinol → HCID 11245187, compound

HRID 2253126Notes

Reaction equation

HRID 2253126 reaction equation
C(O[C:6]([C:8]1[N:9]=[C:10]([Cl:23])[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][C:14]([O:19][CH:20]([CH3:22])[CH3:21])=[CH:13][CH:12]=2)=[O:7])CCC.[NH2:24][CH:25]([CH2:28][OH:29])[CH2:26][OH:27]>C(O)C>[OH:27][CH2:26][CH:25]([NH:24][C:6]([C:8]1[N:9]=[C:10]([Cl:23])[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][C:14]([O:19][CH:20]([CH3:21])[CH3:22])=[CH:13][CH:12]=2)=[O:7])[CH2:28][OH:29]

Participants

4

Reactant 2

HCID 68294SerinolHCID 18698144HCID 18698144, compound

Product 1

HCID 11245187HCID 11245187, compoundYield 114.3%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

0.035 gm of 1-chloro-4-hydroxy-6-isopropoxy-isoquinoline-3-carboxylic acid butyl ester and 0.088 g of 2-amino-propane-1,3-diol were dissolved in 1 ml of ethanol and the mixture was refluxed for 24 h. The reaction mixture was concentrated and the residue was dissolved in 10 ml of ethyl acetate. The ethyl acetate solution was extracted with 5 ml of aqueous 1 M HCl and water, dried (sodium sulfate) and concentrated to give 0.042 g of a white solid: MS-(+)-ion: 355.1.

Workup

  1. temperaturethe mixture was refluxed for 24 h
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe residue was dissolved in 10 ml of ethyl acetate
  4. extractionThe ethyl acetate solution was extracted with 5 ml of aqueous 1 M HCl and water
  5. dry with materialdried (sodium sulfate)
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-574471410e0e4201b1d133cd7e5817cb
Source dataset
uspto-grants-2008_01
Patent number
US07323475B2

Reaction notes

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