HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 8-Bromo-11-ethyl-5,11-dihydro-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 5-Bromo-2-chloro-N-[2-(ethylamino)pyridin-3-yl]pyridine-3-carboxamide | HCID 12015728 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 8-Bromo-11-ethyl-5,11-dihydro-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one | HCID 12015729 | 75% |
Reaction Steps
To a solution of 2-chloro-N-{2-(ethylamino)-3-pyridinyl}-5-bromo-3-pyridinecarboxamide (54.9 g, 154.4 mmol) in pyridine (308 mL) at 50° C. was added drop-wise a 1 M solution of NaHMDS (sodium hexamethyldisilazide) in THF (355 mL, 355 mmol). After 10 min, the reaction was allowed to cool to room temperature, and then was poured over ice water (2 L). The resulting solid was filtered, rinsed with water and then hexane. The solid was dried under reduced pressure to give the title compound (36 g, 75% yield) as a dark green solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420359B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-1d89d4079a874fb8bebf53aab3de110b |
| Source note | uspto-grants-2002_07 |