HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 2-Bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methanol tetrahydrofuran water | HCID 21892291 | — |
| Reactant | Methyl 2-bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylate | HCID 57500654 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acid | HCID 57500655 | 13% |
Reaction Steps
Methyl 2-bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylate (1.0 eq, 17 mg, 0.050 mmol) was suspended in a 1:1:1 mixture of MeOH/THF/water (0.6 ml). LiOH (39 mg) was added and the mixture stirred at room temperature for one hour. Water and 6NHCl was added and the resulting precipitate was filtered. The material was purified by preparative HPLC. Genevac evaporation provided 2-bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acid as a solid (2.1 mg, 13% yield). LCMS (ES): >95% pure, m/z 324 [M]+, 326[M+2]+; 1H NMR (DMSO-d6, 400 MHz) δ 7.75 (s, 1H), 7.75 (dd, J=1.6, J=8.0, 1H), 7.90 (d, J=8.4, 1H), 8.03 (d, J=1.6, 1H), 12.06 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910600B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-5423f45479144982b7865cdf8aac3378 |
| Source note | uspto-grants-2011_03 |