Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl Beta-Carboline-3-Carboxylate | HCID 105078 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 3013463 | HCID 3013463 | — |
Reaction Steps
To a stirred solution of ethyl 9H-β-carboline-3-carboxylate (400 mg, 1.67 mmol) in DMF (5 mL) under a nitrogen atmosphere was added NaH (73 mg, 60% in mineral oil, 1.76 mmol) portionwise, followed by 4-methylbenzyl bromide (308 mg, 1.67 mmol). Stirring was continued for 48 hours at ambient temperature, water (50 mL) was then added to the mixture. The precipitate was filtered, washed with water and dried to give a solid that was dissolved in methanol (35 mL). To the resulting solution, NaOH (2N, 1 mL) and H2NOH (35 mL, 50 wt. % solution in H2O, 0.53 mol) were added. The suspension was stirred for 7 days at ambient temperature. The mixture was then filtered and dried to the title product (0.20 g, 36%). 1H NMR (400 MHz, DMSO-d6): δ 11.25 (1H, s), 8.95–9.03 (2H, m), 8.83 (1H, s), 8.45 (1H, d, J=8 Hz), 7.05–7.81 (7H, m), 5.78 (2H, s), 2.21 (3H, s). HRMS (M+H)+ found: 332.1400. Calcd for C20H18N3O2: 332.1399.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07001912B2 |
|---|
| Source dataset | uspto-grants-2006_02 |
|---|
| ORD ID | ord-f76710a2ee704eb5b9d02c45aa8dfe69 |
|---|
| Source note | uspto-grants-2006_02 |
|---|