HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Benzyl-1-oxa-6-azaspiro(2,5)octane → HCID 54673547, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Benzyl-1-oxa-6-azaspiro(2,5)octane | HCID 89238 | — |
| Reactant | HCID 178515818 | HCID 178515818 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Solvent | Ethanol hydrochloride | HCID 21887872 | — |
| Product | HCID 54673547 | HCID 54673547 | 78.5% |
Reaction Steps
Referring to the method 2 of Example 1, N-benzyl-1-oxa-6-azaspiro[2,5]-octane and 5-bromo-2-hydroxy-pyridine were used for preparing a free base. Melting point: 146-148° C. The product was dissolved in ethanol-ethyl acetate and salified with HCl-EtOH to obtain a hydrochloride, yield 78.5%. Melting point: 148-150° C. 1H-NMR (D2O, ppm) δ: 7.594 (1H, d, J=2.80 Hz), 7.495 (1H, dd, J1=9.52 Hz, J2=2.52 Hz), 7.24-7.34 (5H, m), 6.365 (1H, d, J=9.52 Hz), 4.112 (2H, s), 3.891 (2H, s), 3.208 (2H, d, J=13.15 Hz), 3.031 (2H, t, J1=11.20 Hz, J2=12.60 Hz), 1.742 (2H, t×d, J1=11.20 Hz, J2=3.95 Hz), 1.573 (2H, J=14.57 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921563B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-742294f5d54b447bb32b20c922119df3 |
| Source note | uspto-grants-2014_12 |