HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → HCID 71255279, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | N-Methylethylenediamine | HCID 8014 | — |
| Reactant | 2,4-Dichloroquinoline | HCID 607503 | — |
| Reactant | 2,3,4,5-Tetrahydro-1H-benzo[c]azepine | HCID 10464472 | — |
| Reactant | 2,4,6-Trichloroquinoline | HCID 18796691 | — |
| Product | HCID 71255279 | HCID 71255279 | — |
Reaction Steps
The title compound was prepared in analogy to Example 118-1 in Scheme 59 by using 2,3,4,5-tetrahydro-1H-2-benzazepine (commercial available), 2,4-dichloroquinoline (commercial available) and N-methyl-ethane-1,2-diamine (commercial available) instead of 7-bromo-2,3,4,5-tetrahydro-1H-2-benzazepine, 2,4,6-trichloroquinoline and ethane-1,2-diamine respectively. MS obsd. (ESI+) [(M+H)+] 347. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.42 (brs, 2 H), 7.88 (s, 1 H), 7.55 (d, J=6.4 Hz, 1 H), 7.47 (s, 2 H), 7.16-7.11 (m, 4 H), 6.01 (s, 1 H), 4.87 (s, 2 H), 4.14 (s, 2 H), 3.63 (s, 2 H), 3.20 (t, J=5.6 Hz, 2 H), 3.02 (s, 2 H), 2.67 (s, 3 H), 1.80 (s, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871756B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-48c27dae38754038a1f5b8107522f2ac |
| Source note | uspto-grants-2014_10 |