Dibenzylamine → HCID 54341854, compound
Reaction equation
C(O[CH2:5][CH:6]=[CH:7][CH2:8][N:9]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=O)C.[CH2:22]([NH:29][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[C:16]1([N:9]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:8][CH:7]=[CH:6][CH2:5][N:29]([CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
3
Procedure
Following the general procedure of Example 11 by replacing 1-acetoxy-4-dibenzylamino-2-butene with 1-acetoxy-4-diphenylamino-2-butene and replacing dicyclohexylmethylamine with dibenzylamine, the title compound is obtained as a white solid.
Sources & evidence
- ORD record
- ord-26f20aa301a147ddbf8b176b1b7b59cb
- Source dataset
- uspto-grants-1994_02
- Patent number
- US05283367
Reaction notes
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