Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 85628847 | HCID 85628847 | — |
| Product | HCID 22252938 | HCID 22252938 | 74% |
Reaction Steps
A solution of 9H-1-thia-9,10-diaza-cyclopenta[b]fluorene-4-carboxylic acid, methyl ester, (0.025 g, 0.089 mM) in 3 mL DMF was added to a 60% NaH mineral oil dispersion (0.007 g, 0.178 mM) at room temperature. Following cessation of gas evolution, benzyl bromide (0.012 mL, 0.017 g, 0.098 mM) was added and the mixture stirred at room temperature for 3.5 h. 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, and concentrated in vacuo to afford 0.013 g of an oily solid that was identified as unreacted 9H-1-thia-9,10-diaza-cyclopenta[b]fluorene-4-carboxylic acid, methyl ester. Adjusted the above aqueous layer from the initial reaction workup to pH 1 with 1N HCl, and extracted with ethyl acetate (4×25 mL). The combined ethyl acetate extracts were washed with H2O, 1N HCl, and saturated brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 0.023 g (74%) of the title compound 9-benzyl-9H-1-thia-9,10-diaza-cyclopenta[b]fluorene-4-carboxylic acid as a yellow solid (MW 358.42, C21H14N2O2S).
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-967de8b5f77c470da8b853d4f289f8a9 |
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| Source note | uspto-grants-2006_01 |
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