2-Thiophenecarboxaldehyde → HCID 57434517, compound
Reaction equation
[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2C=C[C:17](C)=[CH:16][CH:15]=2)[O:6][C:7]=1[C:8]1C=CC=CC=1.C/C(/C(C)=O)=N\O.[S:28]1C=CC=C1C=O>>[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2[S:28][CH:17]=[CH:16][CH:15]=2)[O:6][C:7]=1[CH3:8]Participants
4
Procedure
Analogously to the building block synthesis of 4-iodomethyl-5-phenyl-2-p-tolyl-oxazole, diacetylmonoxime and thiophene-2-carbaldehyde gave 4-iodomethyl-5-methyl-2-thiophen-2-yloxazole.
Sources & evidence
- ORD record
- ord-6fa4f59536424fabb7e0dcb29fbb4866
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07335671B2
Reaction notes
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