HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofurfurylamine → HCID 59553308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofurfurylamine | HCID 253298 | — |
| Reactant | 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide | HCID 59553095 | — |
| Product | HCID 59553308 | HCID 59553308 | — |
Reaction Steps
Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and C-(tetrahydro-furan-2-yl)-methylamine according to conditions described in general procedure C. Mp: 103-105° C.; 1H NMR (400 MHz, CDCl3) δ 1.55-1.80 (m, 4 H), 3.21 (t, J=4.4 Hz, 4 H), 3.45-3.89 (m, 5 H), 3.83 (t, J=4.8 Hz, 4 H), 5.42 (s, 1 H), 6.06 (s, 1 H), 6.75 (d, J=11.7 Hz, 1H), 7.07 (d, J=8.0 Hz, 1 H), 7.22 (d, J=8.4 Hz, 1H), 7.30 (s, 1 H), 7.42-7.52 (m, 2 H), 7.77-7.94 (m, 3 H), 8.11 (s, 1 H), 8.40 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114873B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-3e1cccbc57fa49eda9e2d2263db14cc7 |
| Source note | uspto-grants-2012_02 |