p-Toluenesulfonic acid → Desmethylnitrazolam

HRID 1764535Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1764535
[NH:1]([C:3]1[CH2:9][N:8]=[C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[C:6]2[CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=[CH:19][C:5]=2[N:4]=1)[NH2:2].N[C:24]1CN=C(C2C=CC=CC=2)C2C=C([N+]([O-])=O)C=CC=2N=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C([O-])([O-])OCC.C(Cl)(Cl)Cl>[N+:20]([C:17]1[CH:18]=[CH:19][C:5]2[N:4]3[CH:24]=[N:2][N:1]=[C:3]3[CH2:9][N:8]=[C:7]([C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:6]=2[CH:16]=1)([O-:22])=[O:21]

Komponenten

6

Versuchsvorschrift

2-Hydrazino-7-nitro-5-phenyl-3H-1,4-benzodiazepine prepared from 5.6 parts of 2-amino-7-nitro-5-phenyl-3H-1,4-benzodiazepine in a similar manner to Example 7, is dissolved in a mixture of 20 parts by volume of ethyl orthoformate and 100 parts by volume of chloroform, followed by the addition of 10 parts of p-toluenesulfonic acid. The whole mixture is left standing at room temperature for 1 hour with occasional shaking. After completion of the reaction, the solution is washed with a saturated aqueous solution of sodium bicarbonate, then with water, and dried over sodium sulfate. After evaporation of the solvent, the residue is treated with ethyl acetate, whereby 8-nitro-6-phenyl-4H-s-triazolo [4,3-a][1,4] benzodiazepine is yielded as crystals. Recrystallization from tetrahydrofuran yields pale yellow needles melting at 271° C to 272° C.

Aufarbeitung

  1. waitThe whole mixture is left
  2. customAfter completion of the reaction
  3. washthe solution is washed with a saturated aqueous solution of sodium bicarbonate
  4. dry with materialwith water, and dried over sodium sulfate
  5. customAfter evaporation of the solvent
  6. additionthe residue is treated with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-533073bec3c2449e8f00ad737e7484a5
Quelldatensatz
uspto-grants-1978_09
Patentnummer
US04116956

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