Water → HCID 20237819, compound

HRID 1903799Notes

Reaction equation

HRID 1903799 reaction equation
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH:2]1[O:4][CH2:3]1.[CH3:12][O:13][C:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17]([NH:24][CH2:25][CH2:26][NH2:27])=[N:16][CH:15]=1.O>CN(C)C=O>[O:5]([CH2:1][CH:2]([OH:4])[CH2:3][NH:27][CH2:26][CH2:25][NH:24][C:17]1[C:18]2[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:14]([O:13][CH3:12])=[CH:15][N:16]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

Participants

5

Procedure

5.2 g. Phenyl glycidyl ether and 15 g. 4-methoxy-1-(2-aminoethylamino)-isoquinoline are dissolved in dimethylformamide and left to stand for 72 hours at ambient temperature. The reaction mixture is then poured into water, extracted with methylene chloride, dried and purified chromatographically on a silica gel column using, as elution agent, methylene chloride-methanol-triethylamine (8:1:0.05 v/v/v). By evaporation of the pure fractions, there are obtained 5.5 g. (44% of theory) of an oil. By the addition of 1.7 g. fumaric acid to a solution of this oil in ethyl acetate-ethanol, a hydrogen fumarate is precipitated out and this is then recrystallized from isopropyl alcohol. The desired product is obtained in the form of colorless cyrstals; m.p. 152°-153° C.

Workup

  1. waitleft
  2. extractionextracted with methylene chloride
  3. customdried
  4. custompurified chromatographically on a silica gel column
  5. washusing, as elution agent, methylene chloride-methanol-triethylamine (8:1:0.05 v/v/v)
  6. customBy evaporation of the pure fractions, there
  7. customare obtained 5.5 g
  8. additionBy the addition of 1.7 g
  9. customfumaric acid to a solution of this oil in ethyl acetate-ethanol, a hydrogen fumarate is precipitated out
  10. customthis is then recrystallized from isopropyl alcohol

Sources & evidence

ORD record
ord-59cd52a6ab394524a3bb8b5b3d657343
Source dataset
uspto-grants-1984_03
Patent number
US04438128

Reaction notes

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