Hydrazine → 6,7-Dihydro-2-methyl-7-(4-aminobenzoyl)-5H-pyrimido-[5,4-d][1]benzazepine
Reaction equation
[CH3:1][C:2]1[N:3]=[CH:4][C:5]2[CH2:6][CH2:7][N:8]([C:17](=[O:27])[C:18]3[CH:23]=[CH:22][C:21]([N+:24]([O-])=O)=[CH:20][CH:19]=3)[C:9]3[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=3[C:11]=2[N:12]=1.NN>C(O)C.[Pd]>[CH3:1][C:2]1[N:3]=[CH:4][C:5]2[CH2:6][CH2:7][N:8]([C:17](=[O:27])[C:18]3[CH:19]=[CH:20][C:21]([NH2:24])=[CH:22][CH:23]=3)[C:9]3[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=3[C:11]=2[N:12]=1Participants
5
Procedure
A mixture of 400 mg of 6,7-dihydro-2-methyl-7-(4-nitrobenzoyl)-5H-pyrimido(5,4-d][1]benzazepine, 87 μl of anhydrous hydrazine and 40 mg of 10% Pd/C in 22 ml of ethyl alcohol is heated at reflux for 1.25 hours, filtered through diatomaceous earth and the pad washed well with methyl alcohol. The combined filtrates are evaporated in vacuo to a residue which is dissolved in ethyl acetate and filtered through a pad of hydrous magnesium silicate and the filtrate concentrated in vacuo to a residue which is dissolved in methyl alcohol and evaporated again to give 330 mg of the desired product as a yellow foam. HR FABMS: Exact mass (M+H): 331.1555.
Workup
- temperatureis heated
- temperatureat reflux for 1.25 hours
- filtrationfiltered through diatomaceous earth
- washthe pad washed well with methyl alcohol
- customThe combined filtrates are evaporated in vacuo to a residue which
- dissolutionis dissolved in ethyl acetate
- filtrationfiltered through a pad of hydrous magnesium silicate
- concentrationthe filtrate concentrated in vacuo to a residue which
- dissolutionis dissolved in methyl alcohol
- customevaporated again
Sources & evidence
- ORD record
- ord-db670b2769cc494985f432137c7cc760
- Source dataset
- uspto-grants-1998_07
- Patent number
- US05786353
Reaction notes
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