HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3,5-difluorobenzene → HCID 10216263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3,5-difluorobenzene | HCID 136313 | — |
| Reactant | N-(7-chloroquinolin-4-yl)cyclohexane-1,4-diamine | HCID 18391686 | — |
| Reactant | HCID 69921757 | HCID 69921757 | — |
| Product | HCID 10216263 | HCID 10216263 | — |
Reaction Steps
The titled compound was prepared according to the methods described in Example 140, substituting 5-bromo-m-xylene for 1-bromo-3,5-difluorobenzene and (1S,2R,4S,5R)-N-(7-chloroquinolin-4-yl)-2,5-dimethylcyclohexane-1,4-diamine for N-(7-chloroquinolin-4-yl)cyclohexane-1,4-diamine. 1H NMR (300 MHz, DMSO) δ ppm 8.89 (d, 1 H), 8.56 (m, 2 H), 7.92 (d, 1 H), 7.82 (dd, 1 H), 6.99 (d, 1 H), 6.31 (s, 2 H), 6.17 (s, 1 H), 4.10 (br.s, 2 H), 2.14 (s, 6 H), 2.03-2.33 (m, 4 H), 1.69 (m, 2 H), 0.97 (br.d, 6 H). MS(ESI(+)Q1MS m/z 408 (M+H)+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818772B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-4b3f55ddbb334167bef2a97ad2aada76 |
| Source note | uspto-grants-2004_11 |