Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 69269583 | HCID 69269583 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22142171 | HCID 22142171 | — |
Reaction Steps
To a light brown solution of 6-methoxy-8-(4-methyl-[1,4]diazepan-1-yl)-4-(2-trimethylsilanyl-ethoxymethoxy)-quinoline-2-carboxylic acid methyl ester (1.00 g, 2.10 mmol) in 18 mL 3:1:1 tetrahydrofuran:methanol:water was added lithium hydroxide monohydrate (0.267 g, 6.35 mmol). The reaction mixture was stirred at room temperature for 5 hours, acidified to pH 4 with 1 N HCl, and stirred an additional 20 minutes. The reaction mixture was concentrated and dried under high vacuum to afford an orange foam. 1H NMR (300 MHz, DMSO, d6) δ 11.06 (s, 1 H, NH), 7.53 (s, 1 H, C═CH), 7.00 (d, 1 H, Jm=2.4 Hz, ArH5), 6.70 (d, 1 H, Jm=2.4 Hz, ArH7), 4.05-3.99 (m, 2 H, ArNCH2CH2CH2NCH3), 3.87 (s, 3 H, OCH3), 3.68-3.60 (m, 2 H, ArNCH2CH2NCH3), 3.54-3.47 (m, 2 H, ArNCH2CH2NCH3), 3.41-3.26 (m, 2 H, ArNCH2CH2CH2NCH3), 2.82 (d, 3 H, J=4.8 Hz, NCH3), 2.46-2.41 (m, 1 H ArNCH2CH2CH2NCH3), 2.30-2.25 (m, 1 H ArNCH2CH2CH2NCH3); Mass Spec.: calc. for [C17H21N3O4+H]+ Theor. m/z=332; Obs. 332.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045514B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-94c177460dd14c01abcec2d9b04869ac |
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| Source note | uspto-grants-2006_05 |
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