HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzoxazole → 2-(1,4-Diazepan-1-yl)benzo[d]oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(1,4-Diazepan-1-yl)benzo[d]oxazole | HCID 22142317 | 38.7% |
Reaction Steps
In a 40 mL vial at room temperature, 2-chlorobenzo[d]oxazole (760 mg, 5 mmol) was added to a solution of homopiperazine (2 g, 20 mmol) in CH3CN. The reaction mixture gradually turned into a suspension. Upon standing for additional half an hour, solid was filtered off and the collected filtrate was directly subjected to chromatography (Isco, gradient elution, CH2Cl2 to 9:1 CH2Cl2/MeOH). 420 mg of the desired product was isolated (MS, M++H=218.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088928B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-23e66f559d99498d9ed6f091d49d9716 |
| Source note | uspto-grants-2012_01 |