Pyrrole → HCID 20553431, compound
Reaction equation
Cl.Cl[CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]2[C:19]([CH:20]=1)=[N:18][C:17]1[C:12](=[CH:13][CH:14]=[C:15]([O:21][CH2:22][CH2:23][CH2:24]Cl)[CH:16]=1)[CH:11]=2.[NH:26]1[CH:30]=[CH:29][CH:28]=[CH:27]1>>[N:26]1([CH2:3][CH2:4][CH2:5][O:6][C:7]2[CH:8]=[CH:9][C:10]3[C:19]([CH:20]=2)=[N:18][C:17]2[C:12](=[CH:13][CH:14]=[C:15]([O:21][CH2:22][CH2:23][CH2:24][N:26]4[CH:30]=[CH:29][CH:28]=[CH:27]4)[CH:16]=2)[CH:11]=3)[CH:30]=[CH:29][CH:28]=[CH:27]1Participants
3
Procedure
The compound is prepared from 3,6-bis(3-chloropropoxy)acridine hydrochloride and pyrrole as described in Example 44.
Sources & evidence
- ORD record
- ord-e9976b3712854532bf9fd7ad72b011b5
- Source dataset
- uspto-grants-1982_02
- Patent number
- US04314061
Reaction notes
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