HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Methyl 6-aminoquinoline-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 6-Aminoquinoline-5-carboxylic acid | HCID 20564290 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 6-aminoquinoline-5-carboxylate | HCID 45089602 | — |
Reaction Steps
A solution of Example 96A (0.43 g, 2.3 mmol), benzene (10 mL), and methanol (4 mL) was treated with TMSCHN2 (2.0 mL, 4.0 mmol, 2.0M solution in hexanes), stirred at room temperature for 90 minutes, quenched with glacial acetic acid, and concentrated. The residue was diluted with ethyl acetate, washed with saturated Na2CO3, dried (MgSO4), filtered, and concentrated to provide the desired product (0.401 g). MS (DCI) m/e 220 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491718B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-1e8b4c0439874300b29d7cb572a86c18 |
| Source note | uspto-grants-2009_02 |