Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-(2,3-Dichlorophenyl)piperazine | HCID 851833 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 21073341 | HCID 21073341 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 21073427 | HCID 21073427 | 63% |
Reaction Steps
To a solution of 4-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-6-yloxy)-butyraldehyde (0.325 g, 1.37 mmol) in dichloroethane (6 mL) was added a solution of 1-(2,3-dichloro-phenyl)-piperazine (0.318 g, 1.37 mmol) in dichloroethane (3 mL) via cannula. The mixture was stirred for 20 minutes at room temperature and NaBH(OAc)3 (0.377 g, 1.78 mmol) was added. The reaction was stirred for 2.5 h and quenched with saturated NaHCO3 and water. The mixture was extracted with EtOAc and the organic layer was washed with saturated NaHCO3, water and brine, dried over Na2SO4 and concentrated. Purification by chromatography on silica gel (0–5% MeOH/CH2Cl2) gave a foam. Et2O was added and product crashed out. The precipitate was filtered and dried to give the title compound as a white solid (0.386 g, 0.854 mmol, 63%). MS: APCI: M+1: 451.1 (Exact Mass: 450.12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160888B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-758e6134150a4bdeaf2a82c0c3f8012f |
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| Source note | uspto-grants-2007_01 |
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