Cyanamide → HCID 10027956, compound
Reaction equation
N#CN.C(O)(=O)C.[NH2:8][C:9]1[N:10]=[C:11]([NH:23][C:24]2[CH:29]=[CH:28][C:27]([O:30][CH2:31][CH2:32][N:33]3[CH2:37][CH2:36][CH2:35][CH2:34]3)=[CH:26][CH:25]=2)[S:12][C:13]=1[C:14]([C:16]1[CH:21]=[CH:20][CH:19]=[C:18](F)[CH:17]=1)=[O:15].BrCC(C1C=CC=C([C:48]([F:51])([F:50])[F:49])C=1)=O>>[NH2:8][C:9]1[N:10]=[C:11]([NH:23][C:24]2[CH:29]=[CH:28][C:27]([O:30][CH2:31][CH2:32][N:33]3[CH2:34][CH2:35][CH2:36][CH2:37]3)=[CH:26][CH:25]=2)[S:12][C:13]=1[C:14]([C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([C:48]([F:51])([F:50])[F:49])[CH:17]=1)=[O:15]Participants
4
Procedure
This compound was prepared from cyanamide, 1-[2-(isothiocyanato-phenoxy)-ethyl]-pyrrolidine of Example 118 and 2-bromo-1-(3-trifluoromethyl-phenyl)-ethanone of Example 127 following a procedure similar to Example 123. Mass spectrum (ES) MH+=477.
Sources & evidence
- ORD record
- ord-213779246b904aab831758ac06bc130e
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06818663B2
Reaction notes
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