Benzoyl chloride → HCID 19068969, compound
Reaction equation
C1(S([N:10]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]3[CH:19]=[C:20]([C:22]([O:24][CH3:25])=[O:23])[S:21][C:11]2=3)(=O)=O)C=CC=CC=1.S1C2NC3C(C=2C=C1C(OC)=O)=CC=CC=3.[H-].[Na+].[C:44](Cl)(=[O:51])[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1>>[C:44]([N:10]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:12]2[CH:19]=[C:20]([C:22]([O:24][CH3:25])=[O:23])[S:21][C:11]1=2)(=[O:51])[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1Participants
5
Procedure
Prepared analogously to (20) from (19) (0.5 g), 0.06 g NaH and 0.46 g benzoyl chloride afforded (0.7 g)(21), m.p. 149.5°-151.2° C.
Sources & evidence
- ORD record
- ord-3126d1859c13494cbf0a32ee8835cb11
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05536721
Reaction notes
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