Benzothiazole → 1-(Benzothiazol-2-ylmethyl)-5-bromo-2-chlorobenzene
Reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.[Br:10][C:11]1[CH:12]=[CH:13][C:14]([Cl:19])=[C:15]([CH:18]=1)[CH:16]=O>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH2:16][C:15]1[CH:18]=[C:11]([Br:10])[CH:12]=[CH:13][C:14]=1[Cl:19]Participants
3
Procedure
Benzothiazole and 5-bromo-2-chlorobenzaldehyde obtained in Reference Example 16-(1) were treated in a manner similar to Reference Example 100 to give the target compound. APCI-Mass m/Z 338/340 (M+H).
Workup
- additionwere treated in a manner similar to Reference Example 100
- customto give the target compound
Sources & evidence
- ORD record
- ord-1a32fb9998db460aa30b8df7e592b945
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08222219B2
Reaction notes
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