Water → HCID 54345162, compound

HRID 1903785Notes

Reaction equation

HRID 1903785 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.NC[CH2:14][NH:15][C:16]1[CH:24]=[CH:23][CH:22]=[C:21]2[C:17]=1[CH:18]=[N:19][NH:20]2.C[N:26]([CH3:29])[CH:27]=O.[OH2:30]>C(Cl)Cl>[C:3]([O:4][CH:2]([CH2:29][NH:26][CH2:27][CH2:14][NH:15][C:16]1[CH:24]=[CH:23][CH:22]=[C:21]2[C:17]=1[CH:18]=[N:19][NH:20]2)[CH2:1][O:5][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)(=[O:30])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

Participants

6

Procedure

3.0 g. Phenyl glycidyl ether and 7.0 g. 4-(2-aminoethylamino)-indazole are dissolved in 7 ml. dimethylformamide by warming and then left to stand for 20 hours at ambient temperature. The reaction mixture is dissolved in methylene chloride, shaken out 10 times with water and dried with anhydrous sodium sulphate. The solution is treated with fullers' earth, evaporated and the residue is dissolved in ethyl acetate and 3.0 g. benzoic acid added thereto. The salt obtained is recrystallized from isopropyl alcohol, with the addition of active charcoal and fuller's earth. There are obtained 3.9 g. (43% of theory) of the desired product in the form of colorless crystals; m.p. 155°-156° C.

Workup

  1. waitleft
  2. dry with materialdried with anhydrous sodium sulphate
  3. additionThe solution is treated with fullers' earth
  4. customevaporated
  5. dissolutionthe residue is dissolved in ethyl acetate
  6. additionbenzoic acid added
  7. customThe salt obtained
  8. customis recrystallized from isopropyl alcohol, with the addition of active charcoal and fuller's earth
  9. customThere are obtained 3.9 g

Sources & evidence

ORD record
ord-f1e50dacf22345bcb255d6da92d2ffd4
Source dataset
uspto-grants-1984_03
Patent number
US04438128

Reaction notes

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