HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 3-Fluoro-5-morpholin-4-yl-N-{4-[(2-pyrrolidin-1-ylpyrimidin-4-yl)oxy]-1-naphthyl}benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide | HCID 59553095 | — |
| Product | 3-Fluoro-5-morpholin-4-yl-N-{4-[(2-pyrrolidin-1-ylpyrimidin-4-yl)oxy]-1-naphthyl}benzamide | HCID 59553075 | — |
Reaction Steps
Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and pyrrolidine according to conditions described in general procedure C. Mp: 205-207° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.81 (s, 4 H), 3.06 s, 2 H), 3.27 (s, 4 H), 3.41 (s, 2 H), 3.77 (s, 4 H), 6.27-6.19 (m, 1 H), 7.03-7.06 (m, 1 H), 7.27 (d, J=9.1Hz, 1 H), 7.42-7.46 (m, 1 H), 7.51 (s, 1 H), 7.57-7.639 (m, 3 H), 7.86 (d, J=8.4 Hz, 1 H), 8.00 (d, J=8.3 Hz, 1 H), 8.23-8.25 (m, 1 H), 10.47 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829560B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-69971b269f994ff3859f1891e1846439 |
| Source note | uspto-grants-2010_11 |