HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-o-xylene → HCID 11645379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-o-xylene | HCID 68472 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Product | HCID 11645379 | HCID 11645379 | — |
Reaction Steps
The title compound was prepared from commercially available ethyl isonipecotate, 2,3-dimethylbromobenzene as the aryl halide, and 4-hydroxypiperidine as the secondary amine utilizing general procedures A and B described above. 1H NMR (300 MHz, CDCl3) δ 7.06 (d, J=7.7 Hz, 1H), 6.90 (d, J=7.7 Hz, 2H), 4.12 (m, 1H), 3.96 (m, 1H), 3.83 (m, 1H), 3.33-3.13 (m, 4H), 2.70-2.61 (m, 3H), 2.27 (s, 3H), 2.22 (s, 3H), 2.12-1.43 (m, 8 H). ESI MS: 317.4 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604190B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-ac1530493cb744a3a46a05adba54f853 |
| Source note | uspto-grants-2013_12 |