Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | alpha-Bromo-2-nitrotoluene | HCID 77569 | — |
| Reactant | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| Reactant | HCID 69461240 | HCID 69461240 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69461264 | HCID 69461264 | 35% |
Reaction Steps
To a solution of 920 μl (1.84 mmol) of 2M LDA/THF in 5 ml of anhydrous THF, add dropwise at −78° C. under an inert atmosphere a solution of 300 mg (0.92 mmol) of 1-ethyl-7,8-dimethoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one (IIbd) in 2 ml of THF. Allow to equilibrate to room temperature for 30 minutes. Add dropwise at −30° C. a solution of 220 mg (1.01 mmol) of 2-nitrobenzyl bromide in 2 ml of THF. Stir at room temperature for 12 hours. Add 1 ml of H2O. Evaporate the THF. Purify by silica chromatography (AcOEt 1/hexane 4, 1/1, then AcOEt). Recrystallize in EtOH/cHexane. Yield: 35%. M: 158–160° C. 1H-NMR (DMSO, 300 MHz): d 0.87–0.91 (m, 3H, CH3), 3.61–3.99 (m, 10H, NCH+CHCH2+2OCH3), 4.35–4.40 (m, 1H, NCH), 6.60 (s, 1H Ar), 6.82 (s, 1 H Ar), 7.37–7.90 (m, 9H Ar). Mass: (M+H)+=460.88.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250410B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-a00ba59825d348269d2e3566080be1b9 |
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| Source note | uspto-grants-2007_07 |
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