HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluoro-2-(trifluoromethyl)benzyl bromide → 1-(5-Fluoro-2-trifluoromethylbenzyl)-7-iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluoro-2-(trifluoromethyl)benzyl bromide | HCID 2737578 | — |
| Reactant | 7-iodo-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-one | HCID 44829114 | — |
| Product | 1-(5-Fluoro-2-trifluoromethylbenzyl)-7-iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one | HCID 57885880 | 51% |
Reaction Steps
7-Iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one (1.07 g) was reacted with 5-fluoro-2-trifluoromethylbenzyl bromide as in General Procedure 1 to give the title compound as an off-white solid (51% yield). M.p. 244-245° C., LCMS: m/z=453.03 (M+H+), 1H-NMR (DMSO-d6, 400 MHz) δ 4.21 (s, 2H), 5.15 (s, 2H), 6.97 (s, 1H0, 7.12 (d, J=9.8 Hz, 1H), 7.25 (s, 1H), 7.36 (dd, J=8.3 Hz, 1H), 7.84 (s, 1H), 7.88-7.94 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080561B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-8011bd0f352245789b6e3ba0cd7183ef |
| Source note | uspto-grants-2011_12 |