Tributyltin Chloride → HCID 178439891, compound
Reaction equation
[CH3:1][C:2]1[C:10]2[N:9]=[C:8]([CH2:11][CH2:12][CH3:13])[N:7]([CH2:14][C:15]3[CH:16]=[CH:17][C:18]([C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=4[C:27]#[N:28])=[N:19][CH:20]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[N-:29]=[N+:30]=[N-:31].[Na+].C([Sn](Cl)(CCCC)CCCC)CCC>>[CH3:1][C:2]1[C:10]2[N:9]=[C:8]([CH2:11][CH2:12][CH3:13])[N:7]([CH2:14][C:15]3[CH:16]=[CH:17][C:18]([C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=4[C:27]4[NH:31][N:30]=[N:29][N:28]=4)=[N:19][CH:20]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
A mixture of 4-methyl-2-propyl-1-[[2-(2-cyanophenyl)-5-pyridinyl]methyl]-1H-benzimidazole (0.87 g, 2.39 mmol), NaN3 (0.77 g, 11.94 mmol), and tri-n-butyltin chloride (3.88 g, 11.94 mmol) in xylenes (20 mL) was heated under reflux for 20 h. The reaction mixture was concentrated and 2N HCl was added. The mixture was extracted with ether (discarded) and adjusted to pH 5 with 50% NaOH. The aqueous phase was extracted with CH2Cl2, and the extracts were washed with water, dried, and concentrated. Purification by flash chromatography (5% MeOH/CH2Cl2) and recrystallization from EtOH/EtOAc/ether gave 0.45 g (45%) of product as a white solid, mp 169°-170° C.
Workup
- temperaturewas heated
- temperatureunder reflux for 20 h
- concentrationThe reaction mixture was concentrated
- addition2N HCl was added
- extractionThe mixture was extracted with ether (discarded)
- extractionThe aqueous phase was extracted with CH2Cl2
- washthe extracts were washed with water
- customdried
- concentrationconcentrated
- customPurification
- customby flash chromatography (5% MeOH/CH2Cl2) and recrystallization from EtOH/EtOAc/ether
Sources & evidence
- ORD record
- ord-462af2e3b7b9473eb48be648632261f0
- Source dataset
- uspto-grants-1995_09
- Patent number
- US05451583
Reaction notes
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