1-methyl-1H-1,3-benzodiazole-2-carbaldehyde → HCID 18366587, compound
Reaction equation
[CH3:1][N:2]1[C:7](=[O:8])[C:6]2[CH:9]=[CH:10][S:11][C:5]=2[N:4]([CH2:12][CH:13]2[CH2:15][CH2:14]2)[C:3]1=[O:16].[CH3:17][N:18]1[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=2[N:20]=[C:19]1[CH:27]=[O:28]>>[CH:13]1([CH2:12][N:4]2[C:5]3[S:11][C:10]([CH:27]([OH:28])[C:19]4[N:18]([CH3:17])[C:22]5[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=5[N:20]=4)=[CH:9][C:6]=3[C:7](=[O:8])[N:2]([CH3:1])[C:3]2=[O:16])[CH2:14][CH2:15]1Participants
3
Procedure
The title compound was prepared from 3-Methyl-1-(cyclopropylmethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (Example 32 step a) and 1-methylbenzimidazole-2-carboxaldehyde following the method of Example 1 step d.
Sources & evidence
- ORD record
- ord-405c4dbcc62342c884f8326637fe2fba
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300334B1
Reaction notes
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