5-Chloromethyl-3-(3-iodo-benzyl)-[1,2,4]oxadiazole → 5-Chloromethyl-3-(4-iodo-benzyl)-[1,2,4]oxadiazole
Reaction equation
[Cl:1][CH2:2][C:3]1[O:7][N:6]=[C:5]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11](I)[CH:10]=2)[N:4]=1.ONC(=N)CC1C=CC([I:26])=CC=1>>[Cl:1][CH2:2][C:3]1[O:7][N:6]=[C:5]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([I:26])=[CH:11][CH:10]=2)[N:4]=1Participants
3
Procedure
The title compound is prepared essentially as described for 5-chloromethyl-3-(3-iodo-benzyl)-[1,2,4]oxadiazole, employing N-hydroxy-2-(4-iodo-phenyl)-acetamidine. LC-MS (m/e): 335 (M+1).
Sources & evidence
- ORD record
- ord-3f0d2d3373444ac5b6e691d564401b32
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07803938B2
Reaction notes
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