Allylamine → HCID 178457002, compound

HRID 1980667Notes

Reaction equation

HRID 1980667 reaction equation
CO[C:3]1[C:7](OC)=[N:6][S:5](=[O:11])(=[O:10])[N:4]=1.[CH3:12][N:13]([CH2:15][C:16]1[O:20][C:19]([CH2:21][S:22][CH2:23][CH2:24][NH2:25])=[CH:18][CH:17]=1)[CH3:14].[CH2:26]([NH2:29])[CH:27]=[CH2:28]>CO>[CH2:26]([NH:29][C:7]1[C:3]([NH:25][CH2:24][CH2:23][S:22][CH2:21][C:19]2[O:20][C:16]([CH2:15][N:13]([CH3:12])[CH3:14])=[CH:17][CH:18]=2)=[N:4][S:5](=[O:10])(=[O:11])[N:6]=1)[CH:27]=[CH2:28]

Participants

5

Reactant 3

HCID 7853AllylamineHCID 1622035-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamineHCID 122305383,4-Dimethoxy-1,2,5-thiadiazole 1,1-dioxide

Product 1

HCID 178457002HCID 178457002, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

To a partial suspension of 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide (2.08 g; 11.7 mmoles) in 200 ml of methanol that had been cooled to 0° in an ice-water bath was added dropwise over a period of 45 minutes a solution of 2-[(5-dimethylaminomethyl-2-furyl)methylthio]ethylamine in 30 ml of methanol. When the addition was completed, 10.5 ml of allylamine was added and the solution was allowed to stir at ambient temperature for 18 hours. The reaction mixture was evaporated under reduced pressure and the residue was placed on 120 g of silica gel and chromatographed using a gradient elution of methylene chloride-methanol. The appropriate fractions were combined, evaporated under reduced pressure and the residue crystallized with isopropyl alcohol to give the title compound, mp 83°-86°; the NMR spectrum (100 MHz) in d6 dimethyl sulfoxide showed the presence of approximately 0.9 moles of isopropyl alcohol.

Workup

  1. temperaturehad been cooled to 0° in an ice-water bath
  2. additionWhen the addition
  3. customThe reaction mixture was evaporated under reduced pressure
  4. customchromatographed
  5. washa gradient elution of methylene chloride-methanol
  6. customevaporated under reduced pressure
  7. customthe residue crystallized with isopropyl alcohol

Sources & evidence

ORD record
ord-da8c7fc5baa049c4967a4adbf02b5f44
Source dataset
uspto-grants-1985_04
Patent number
US04510309

Reaction notes

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