3,6-Bis(4-chlorobutyryl)-N-ethylcarbazole → HCID 21552925, compound
Reaction equation
ClCCCC(C1C=CC2[N:11]([CH2:26][CH3:27])[C:12]3[C:17]([C:18]=2C=1)=CC(C(=O)CCCCl)=CC=3)=O.Cl[CH2:29][CH2:30][CH:31]([CH3:56])[C:32]([C:34]1[CH:35]=[CH:36][C:37]2[N:38]([CH2:54][CH3:55])[C:39]3[C:44]([C:45]=2[CH:46]=1)=[CH:43][C:42]([C:47](=[O:53])[CH:48]([CH3:52])[CH2:49][CH2:50]Cl)=[CH:41][CH:40]=3)=[O:33]>>[CH2:54]([N:38]1[C:37]2[CH:36]=[CH:35][C:34]([C:32](=[O:33])[CH:31]([CH3:56])[CH2:30][CH2:29][N:11]3[CH2:26][CH2:27][CH2:18][CH2:17][CH2:12]3)=[CH:46][C:45]=2[C:44]2[C:39]1=[CH:40][CH:41]=[C:42]([C:47](=[O:53])[CH:48]([CH3:52])[CH2:49][CH2:50][N:11]1[CH2:12][CH2:17][CH2:18][CH2:27][CH2:26]1)[CH:43]=2)[CH3:55]Participants
3
Procedure
Following the procedure of Example 6, only substituting for 3,6-bis(4-chlorobutyryl)-N-ethylcarbazole the appropriate molar equivalent amount of 3,6-bis(4-chloro-2-methylbutyryl)-N-ethylcarbazole, the desired product is obtained.
Sources & evidence
- ORD record
- ord-1adfef6f23ff44cdbd49c98550b4fefd
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03946021
Reaction notes
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