Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23594015 | HCID 23594015 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23594014 | HCID 23594014 | 172% |
Reaction Steps
A solution of 11-methoxy-5H-benzo[b]carbazole-1-carboxylic acid, methyl ester, (0.458 g, 1.5 mM) in 5 mL DMF was added to a 60% NaH mineral oil dispersion (0.12 g, 3.0 mM, washed twice with hexane) at room temperature. Following cessation of gas evolution, benzyl bromide (0.20 mL, 0.288 g, 1.65 mM) was added and the mixture stirred at room temperature for 4 hours. The mixture was diluted with ethyl acetate and H2O, the solvent layers separated, and the aqueous layer extracted with ethyl acetate (4×25 mL). The combined ethyl acetate extracts were washed with H2O, 1N HCl, saturated aqueous NaHCO3 solution, and saturated brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and triturated with hexanes. The resultant yellow-orange gum was purified by column chromatography on silica gel (elution with 9:1 toluene/ethyl acetate) to afford 0.51 g (86%) of the title compound 5-benzyl-11-methoxy-5H-benzo[b]carbazole-1-carboxylic acid, methyl ester as a yellow-orange foam (MW 395.46).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992100B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-137c6a5162fb43bf870f38be1334b669 |
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| Source note | uspto-grants-2006_01 |
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