4-Chlorothieno[3,2-d]pyrimidine → 4-Chlorothieno[3,2-d]pyrimidine-6-carbaldehyde
Reaction equation
[Cl:1][C:2]1[C:3]2[S:10][CH:9]=[CH:8][C:4]=2[N:5]=[CH:6][N:7]=1.ClC1C=CN=C2C=C([CH:21]=[O:22])SC=12>>[Cl:1][C:2]1[C:3]2[S:10][C:9]([CH:21]=[O:22])=[CH:8][C:4]=2[N:5]=[CH:6][N:7]=1Participants
3
Procedure
Starting from 4-chloro-thieno[3,2-d]pyrimidine (20, scheme 4) and following procedure described above for the synthesis of aldehyde 14 (scheme 3, step 1, example 20), title compound 186 was obtained in 84% yield. LRMS (M+1) 199.0 (100%).
Sources & evidence
- ORD record
- ord-5448f255f280475dbe1bad17f8d6c358
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07772247B2
Reaction notes
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