HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 10134004, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 11825587 | HCID 11825587 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10134004 | HCID 10134004 | 33.2% |
Reaction Steps
To a solution of 11-(2-dimethylamino-ethylcarbamoyl)-benzo[a]phenazine-4-carboxylic acid methyl ester (317 mg) in tetrahydrofuran (18 mL) and 2-propanol (10 mL) at 0° C. was added lithium borohydride (2.0M solution in tetrahydrofuran, 1.97 mL) The reaction mixture was stirred at room temperature overnight, and then quenched with ammonium chloride solution. The reaction mixture was extracted with ethyl acetate, dried (MgSO4) and concentrated in vacuo. The residue was purified using flash chromatography (10% MeOH in dichloromethane) to yield the title compound as a yellow solid (98 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132419B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-e906df01baae4427bc1919cd6b1d5ff9 |
| Source note | uspto-grants-2006_11 |