Hydrazine hydrate (1:1) → HCID 19370315, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH:7]([N:14]2[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][N:22]3C(=O)C4=CC=CC=C4C3=O)[CH2:16][CH2:15]2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:3][CH:2]=1.O.NN>>[NH2:22][CH2:21][CH2:20][N:17]1[CH2:18][CH2:19][N:14]([CH:7]([C:4]2[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:15][CH2:16]1Participants
3
Procedure
The title compound was prepared in a quantitative yield in a similar manner to that described in Preparation 15' by reacting 4-[α-(4-pyridyl)benzyl]-1-(2-phthalimidoethyl)piperazine (prepared as described in Preparation 50') and hydrazine hydrate.
Workup
- customdescribed in Preparation 15'
- customprepared
Sources & evidence
- ORD record
- ord-c09bd1c7695e43e7823ce25b183f8c9f
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05470851
Reaction notes
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