Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-t-butoxycarbonyl-4-(1H-benzimidazol-2-yl)[1,4]diazepane | HCID 18464655 | — |
| Reactant | 2-Isopropoxyethyl Methanesulfonate | HCID 18465045 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18464896 | HCID 18464896 | — |
Reaction Steps
Combine 1-(t-butoxycarbonyl)-4-(1H-benzimidazol-2-yl)[1,4]diazepane (0.54 g, 1.71 mmol), and sodium hydride (0.87 g, 3.48 mmol in dimethylformamide (10 mL). After 30 minutes, add 2-(isopropoxy)ethyl mesylate (0.51 g, 5.5 mmol). Heat to 80° C. After 2 hours, cool the reaction mixture to ambient temperature and partition between dichloromethane and a saturated aqueous sodium bicarbonate solution. Separate the layers and extract the organic layer with brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give 1-(t-butoxycarbonyl)-4-(1-(2-(isopropoxy)ethyl)-1H-benzimidazol-2-yl)[1,4]diazepane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06423704B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-60c0c07409594b89930f76a294a1abfc |
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| Source note | uspto-grants-2002_07 |
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