1-Methyl-1H-pyrrole-2-carbaldehyde → HCID 69427397, compound
Reaction equation
[NH:1]([C:3]1N(CC(C)C)[C:7](=[O:13])[N:6]([CH3:14])[C:5](=[O:15])[CH:4]=1)[NH2:2].[S:16]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[C:18]([CH:25]=O)=[CH:17]1.[CH3:27][N:28]1[CH:32]=[CH:31][CH:30]=[C:29]1[CH:33]=O>>[S:16]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[C:18]([CH2:25][N:2]2[C:33]([C:29]3[N:28]([CH3:27])[CH:32]=[CH:31][CH:30]=3)=[C:4]3[C:3]([CH:20]([CH2:19][CH:18]([CH3:25])[CH3:17])[C:7](=[O:13])[N:6]([CH3:14])[C:5]3=[O:15])=[N:1]2)=[CH:17]1Participants
4
Procedure
This compound was made following the procedure described above, starting with 6-hydrazino-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione, and condensing first with 1-benzothiophene-3-carbaldehyde, followed by 1-methyl-1H-pyrrole-2-carbaldehyde. 447 (M+H).
Sources & evidence
- ORD record
- ord-c0116cd6ee0343c190d4e1e44d87af5a
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285558B2
Reaction notes
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