HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinuclidine, 3-amino-, dihydrochloride → HCID 11544770, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| Reactant | 7-Benzoxazolecarboxylic acid, 2-phenyl- | HCID 11806727 | — |
| Product | HCID 11544770 | HCID 11544770 | 57% |
Reaction Steps
N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-phenylbenzoxazole-7-carboxamide was prepared from 2-phenylbenzoxazole-7-carboxylic acid and 3-aminoquinuclidine dihydrochloride using the method outlined in Step C of Example 7. This compound was obtained in 57% yield as a white solid: mp 179-180° C.; 1H NMR (300 MHz, CDCl3) δ 8.21 (dd, J=7.5, 2.1 Hz, 2H), 8.10 (dd, J=7.8, 1.2 Hz, 1H), 7.92 (dd, J=7.8, 1.2 Hz, 1H), 7.61-7.54 (m, 3H), 7.51-7.46 (m, 2H), 4.38-4.33 (m, 1H), 3.63-3.54 (m, 1H), 3.13-3.05 (m, 2H), 2.23 (q, J=3.0 Hz, 1H), 2.00-1.90 (m, 1H), 1.84-1.73 (m, 2H), 1.71-1.64 (m, 1H); MS (ESI) m/z 348[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781430B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-dc8a88d748604b35b7496c882f6df1c1 |
| Source note | uspto-grants-2010_08 |