HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Bromomethyl)-4-chloro-1-(trifluoromethyl)benzene → HCID 57886085, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Bromomethyl)-4-chloro-1-(trifluoromethyl)benzene | HCID 2778116 | — |
| Reactant | 7-iodo-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-one | HCID 44829114 | — |
| Reactant | HCID 57886049 | HCID 57886049 | — |
| Product | HCID 57886085 | HCID 57886085 | 17% |
Reaction Steps
7-Iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one (968 mg) was reacted with 5-chloro-2-(trifluoromethyl)benzyl bromide as in General Procedure 1. The resulting 1-(2-chloro-5-trifluoromethylbenzyl)-7-iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one was reduced as in General Procedure 2 to give the title compound as an orange solid (17% yield). M.p. 189-191° C., LCMS: m/z=454.08 (M+H+), 1H-NMR (DMSO-d6, 400 MHz) δ 3.28-3.34 (m, 2H), 3.41-3.46 (m, 2H), 4.53 (s, 2H), 6.52 (s, 1H), 6.75 (s, 1H), 7.44 (s, 2H), 7.59 (d, J=8.4 Hz, 1H), 7.82 (d, J=8.6 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919502B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-cf2894e8f8784d75a5d9a3eb13b48c66 |
| Source note | uspto-grants-2011_04 |