Diisopropylethylamine → HCID 22158330, compound
Reaction equation
[O:1]=[C:2]1[N:7]2[C:8]3[C:13]([C:14]([CH2:15][CH2:16][NH2:17])=[C:6]2[CH2:5][CH2:4][CH2:3]1)=[CH:12][CH:11]=[CH:10][CH:9]=3.C(N(C(C)C)CC)(C)C.[CH3:27][N:28]([CH3:38])[C:29]1[CH:37]=[CH:36][C:32]([C:33](Cl)=[O:34])=[CH:31][CH:30]=1>>[CH3:27][N:28]([CH3:38])[C:29]1[CH:37]=[CH:36][C:32]([C:33]([NH:17][CH2:16][CH2:15][C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[N:7]3[C:2](=[O:1])[CH2:3][CH2:4][CH2:5][C:6]=23)=[O:34])=[CH:31][CH:30]=1Participants
4
Procedure
E10 was prepared analogously to E9 from 7 g D4 of EP-0167901, 11.2 ml diisopropylethylamine and 4.5 g 4-dimethylaminobenzoic acid chloride.
Sources & evidence
- ORD record
- ord-601c69efb13a491eb5a0c025046fe33e
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04968699
Reaction notes
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