4-Chlorobenzoyl chloride → 2-Amino-7-(p-chloro-benzoyl)-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]azepine
Reaction equation
Br.Br.[NH2:3][C:4]1[CH:5]=[N:6][C:7]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9][C:8]=2[N:14]=1.[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([C:20](Cl)=[O:21])=[CH:18][CH:17]=1>>[NH2:3][C:4]1[CH:5]=[N:6][C:7]2[CH2:13][CH2:12][N:11]([C:20](=[O:21])[C:19]3[CH:23]=[CH:24][C:16]([Cl:15])=[CH:17][CH:18]=3)[CH2:10][CH2:9][C:8]=2[N:14]=1Participants
3
Procedure
This compound was prepared analogous to Example 29 from 2-amino-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]azepine dihydrobromide and p-chloro-benzoyl chloride.
Sources & evidence
- ORD record
- ord-b8a4f2e97b824071b2a6477b02969d06
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04409220
Reaction notes
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