HCID 21523984, compound → HCID 21523997, compound
Reaction equation
OC1C=C[C:5]([N:8]2[C:16]3C(=CC(OC)=C[CH:15]=3)[CH:10]=[C:9]2C2C=CC=CC=2)=[CH:4]C=1.[OH:25][C:26]1[CH:31]=[CH:30][C:29]([N:32]2[C:40]3[C:35](=[CH:36][C:37]([O:41][C:42](=[O:49])[C:43]4[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=4)=[CH:38][CH:39]=3)[CH:34]=[C:33]2[C:50]2[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=2)=[CH:28][CH:27]=1>>[CH2:5]([N:8]([CH2:16][CH3:15])[CH2:9][CH2:10][O:25][C:26]1[CH:27]=[CH:28][C:29]([N:32]2[C:40]3[C:35](=[CH:36][C:37]([O:41][C:42](=[O:49])[C:43]4[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=4)=[CH:38][CH:39]=3)[CH:34]=[C:33]2[C:50]2[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=2)=[CH:30][CH:31]=1)[CH3:4]Participants
3
Procedure
Following a procedure similar to that described in Example 1E but substituting for 1-(4-hydroxyphenyl)-5-methoxy-2-phenylindole an equivalent amount of 1-(4-hydroxyphenyl)-5-benzoyloxy-2-phenylindole there can be obtained 1-{4-[2-(diethylamino)ethoxy]phenyl}-5-benzoyloxy-2-phenylindole.
Sources & evidence
- ORD record
- ord-f579041558714deabed93e872d243564
- Source dataset
- uspto-grants-1976_07
- Patent number
- US03968121
Reaction notes
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