Dimethylformamide → Benzimidazole
Reaction equation
[C:1]1(Cl)[C:7](=O)[C:6](Cl)=[C:5](Cl)[C:3](=O)[C:2]=1Cl.C[N:14]1[C:18](=O)CCC1.C[N:21](C=O)C>>[N:21]1[C:2]2[CH:3]=[CH:5][CH:6]=[CH:7][C:1]=2[NH:14][CH:18]=1Participants
4
Procedure
Each resin was suspended in DMF (200 μL) and a 1 M solution of the aldehyde in DMF was added (0.20 mmol, 200 μL), followed by a 0.25 M solution of chloranil in NMP (0.20 mmol, 800 μL). The resins were shaken for 18 h, the liquid was drained and the resins were washed successively with 1.2-mL portions of NMP (3×), 1 M DIEA/NMP (2×), NMP (3×), MeOH (3×) and DCM (4×). The reaction block was placed in a vacuum chamber for 30 min in order to dry the resin.
Workup
- washthe resins were washed successively with 1.2-mL portions of NMP (3×), 1 M DIEA/NMP (2×), NMP (3×), MeOH (3×) and DCM (4×)
- waitThe reaction block was placed in a vacuum chamber for 30 min in order
- customto dry the resin
Sources & evidence
- ORD record
- ord-ae8eeecc16424b3db78a4b3c53afff93
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07439258B2
Reaction notes
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