HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2) → 4-chloro-N-(3-dimethylaminophenyl)-3-(6-quinolylcarbonylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2) | HCID 77124 | — |
| Reactant | 4-Chloro-3-(6-quinolylcarbonylamino)benzoyl chloride | HCID 22636128 | — |
| Product | 4-chloro-N-(3-dimethylaminophenyl)-3-(6-quinolylcarbonylamino)benzamide | HCID 9889694 | — |
Reaction Steps
Using an analogous procedure to that described in Example 1, 4-chloro-3-(6-quinolylcarbonylamino)benzoyl chloride was reacted with 3-dimethylaminoaniline dihydrochloride to give the title compound; NMR Spectrum: (DMSOd6) 3.04 (s, 6H), 6.5 (d, 1H), 7.08-7.20 (m, 3H), 7.61-7.64 (m, 1H), 7.74 (d, 1H), 7.92 (d, 1H) 8.1-8.2 (m, 2H), 7.31 (d, 1H), 8.58 (d, 1H), 8.72 (s, 1H), 9.02 (s, 1H) 10.13 (s, 1H), 10.5 (s, 1H); Mass Spectrum: Mass Spectrum: M+H+ 445 and 447.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821965B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-2a3a9d46bda64863b90c20aa31a2236a |
| Source note | uspto-grants-2004_11 |