HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Pyrrolidin-1-YL-ethyl)-1H-indazol-4-ylamine → 3-(4-phenoxyphenyl)-N-[1-(2-pyrrolidin-1-ylethyl)-1H-indazol-4-yl]propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Pyrrolidin-1-YL-ethyl)-1H-indazol-4-ylamine | HCID 11492341 | — |
| Reactant | 3-(4-Phenoxyphenyl)propanoic acid | HCID 22036572 | — |
| Product | 3-(4-phenoxyphenyl)-N-[1-(2-pyrrolidin-1-ylethyl)-1H-indazol-4-yl]propanamide | HCID 11465212 | — |
Reaction Steps
1-(2-pyrrolidin-1-yl-ethyl)-1H-indazol-4-ylamine and 3-(4-phenoxy-phenyl)-propionic acid were processed according as described in Example 3 to provide the title compound. 1H NMR (500 MHz, DMSO-D6) δ ppm 1.84 (m, 2 H), 2.00 (m, 2 H), 2.64 (t, J=7.64 Hz, 2 H), 2.93 (t, J=7.64 Hz, 2 H), 3.06 (m, 2 H), 3.52 (m, 2 H), 3.71 (m, 2 H), 4.74 (t, J=6.08 Hz, 2 H), 6.95 (m, 4 H), 7.11 (m, 1 H), 7.28 (m, 2 H), 7.36 (m, 2 H), 7.49 (m, 1 H), 7.67 (m, 1 H), 8.13 (m, 2 H), 9.95 (s, 1 H); MS (DCI/NH3) m/z 455 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071182B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-ffde62cd866f484f85d9d09b95451b0c |
| Source note | uspto-grants-2006_07 |