Sodium → HCID 19075380, compound

HRID 1975117Notes

Reaction equation

HRID 1975117 reaction equation
[Na].[C:2]([OH:7])(=[O:6])[C:3]([OH:5])=[O:4].Cl[C:9]1[C:10]([C:14]2[CH2:15][N:16]([CH3:20])[CH2:17][CH2:18][CH:19]=2)=[N:11][S:12][N:13]=1>C(O)CCCCCC>[C:2]([OH:7])(=[O:6])[C:3]([OH:5])=[O:4].[CH2:2]([O:7][C:9]1[C:10]([C:14]2[CH2:15][N:16]([CH3:20])[CH2:17][CH2:18][CH:19]=2)=[N:11][S:12][N:13]=1)[CH2:3][CH2:9][CH2:10][CH2:14][CH2:19][CH3:18]

Participants

4

Reactant 2

HCID 5360545SodiumHCID 19075340HCID 19075340, compound

Product 1

HCID 19075380HCID 19075380, compound

Reagents, catalysts & solvents 1

HCID 8129HeptanolSolvent

Conditions

Temperature
50 °C

Procedure

To a solution of sodium (120 mg, 5 mml) in 1-heptanol (10 ml) was added 3-(4-chloro-1,2,5-thiadiazol-3-yl)-1,2,5,6-tetrahydro-1-methylpyridine oxalate (310 mg, 1 mmol). The reaction mixture was stirred at 50° C. for 18 h. After evaporation the residue was dissolved in water and extracted with ethyl acetate. The ethyl acetate phase was dried and evaporated to give an oil. Crystallization as the oxalate salt from acetone gave the title compound. Yield: 270 mg (70%). (M.p. 152° C.; M+ : 295; Compound 21).

Workup

  1. customAfter evaporation the residue
  2. dissolutionwas dissolved in water
  3. extractionextracted with ethyl acetate
  4. dry with materialThe ethyl acetate phase was dried
  5. customevaporated
  6. customto give an oil
  7. customCrystallization as the oxalate salt from acetone

Sources & evidence

ORD record
ord-c4f08d018eb84571aa8dfce75bbac4d1
Source dataset
uspto-grants-1994_02
Patent number
US05284859

Reaction notes

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