Nitrobenzene → HCID 131716088, compound
Reaction equation
[N+](C1C=CC=CC=1)([O-])=[O:2].Br[C:11]1[CH:12]=[C:13]2[C:26]3[C:16]([CH2:17][C@@H:18]4[C@@H:23]([C:24]=3[CH:25]=1)[CH2:22][C@H:21]([NH:27][C:28](=[O:34])[N:29]([CH2:32][CH3:33])[CH2:30][CH3:31])[CH2:20][N:19]4[CH2:35]CC)=[CH:15][N:14]2[Si](C(C)(C)C)(C)C>>[CH2:30]([N:29]([CH2:32][CH3:33])[C:28]([NH:27][C@H:21]1[CH2:22][C@H:23]2[C@@H:18]([CH2:17][CH:16]3[C:26]4[C:13](=[CH:12][C:11]([OH:2])=[CH:25][C:24]2=4)[NH:14][CH2:15]3)[N:19]([CH3:35])[CH2:20]1)=[O:34])[CH3:31]Participants
3
Procedure
With nitrobenzene and 3-(13-bromo-1-tert-butyldimethylsilyl-6-n-propyl-8α-ergolinyl)-1,1-diethylurea:
Sources & evidence
- ORD record
- ord-9ddf945f527b4f6bb4f8fa9f5b49473a
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04863929
Reaction notes
Loading…