HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylbenzoxazole-4-carboxylic acid → N-(1-Methylpiperidin-4-yl)-2-phenylbenzoxazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylbenzoxazole-4-carboxylic acid | HCID 10868369 | — |
| Reactant | 1-Methylpiperidin-4-amine dihydrochloride | HCID 22002536 | — |
| Product | N-(1-Methylpiperidin-4-yl)-2-phenylbenzoxazole-4-carboxamide | HCID 11631388 | 38% |
Reaction Steps
N-(1-Methylpiperidin-4-yl)-2-phenylbenzoxazole-4-carboxamide was prepared from 2-phenylbenzoxazole-4-carboxylic acid and 4-amino-1-methylpiperidine dihydrochloride using the conditions described for Step C in Example 1. This compound was obtained in 38% yield as a white solid; mp 126-128° C.; 1H NMR (300 MHz, CDCl3) δ 9.26 (d, J=7.5 Hz, 1H), 8.25 (m, 2H), 8.19 (d, J=7.7 Hz, 1H), 7.70 (d, J=8.1 Hz, 1H), 7.63-7.53 (m, 3H), 7.46 (t, J=8.0 Hz, 1H), 4.20 (m, 1H), 2.86 (m, 2H), 2.37 (s, 3H), 2.33-2.13 (m, 4H), 1.85-1.73 (m, 2H); MS (APCI) m/z 336 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307094B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-d5290a6a412746dc831adda994fab58c |
| Source note | uspto-grants-2007_12 |