HCID 10986642, compound → HCID 15595109, compound
Reaction equation
[Cl:1][C:2]1[CH:37]=[C:36]([C:38]([F:41])([F:40])[F:39])[CH:35]=[CH:34][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][C:8]([N:11](SN(CCC)CCC)[C:12]([NH:14][C:15](=[O:24])[C:16]2[C:21]([F:22])=[CH:20][CH:19]=[CH:18][C:17]=2[F:23])=[O:13])=[C:7]([F:33])[CH:6]=1.[CH:42]([N:45]([CH:48]([CH3:50])[CH3:49])[S:46]Cl)([CH3:44])[CH3:43]>>[Cl:1][C:2]1[CH:37]=[C:36]([C:38]([F:41])([F:39])[F:40])[CH:35]=[CH:34][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][C:8]([N:11]([S:46][N:45]([CH:48]([CH3:50])[CH3:49])[CH:42]([CH3:44])[CH3:43])[C:12]([NH:14][C:15](=[O:24])[C:16]2[C:21]([F:22])=[CH:20][CH:19]=[CH:18][C:17]=2[F:23])=[O:13])=[C:7]([F:33])[CH:6]=1Participants
3
Procedure
39 was prepared, as a white solid, m.p.: 147°-149° C. in a similar manner to (38). The intermediate compound, di(isopropyl)aminosulphenyl chloride, boiled at 92°-4° C. at 20 Torr.
Sources & evidence
- ORD record
- ord-607ecccd8fb54c49975928f61da1076f
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04672139
Reaction notes
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