HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 178514685, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3,4-diaminobenzenesulfonamide | HCID 2735927 | — |
| Reactant | HCID 10706104 | HCID 10706104 | — |
| Reactant | HCID 12925059 | HCID 12925059 | — |
| Reactant | 3,4-Diaminobenzamide | HCID 21217843 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178514685 | HCID 178514685 | — |
Reaction Steps
The title compound was prepared as described in Example 1 substituting 3,4-diamino-benzenesulfonamide for 3,4-diamino-benzamide and 4-(4-chloro-benzoyl)-benzaldehyde for 4-(2-phenyl-[1,3]dioxolan-2-yl)-benzaldehyde in Step C (reaction mixture was heated to 60° C.). TLC (silica, 1% methanol saturated with ammonia/9% methanol/CH2Cl2): Rf=0.32. HPLC (Method A): Rt=8.03. MS (ESI+): mass calculated for C20H14ClN3O3S, 411.0; m/z found, 412.0 [M+H]+. 1H NMR (500 MHz, DMSO-d6): δ 13.48 (br s, 1H), 8.31 (d, J=8.3 Hz, 2H), 8.16 (br s, 1H), 7.88 (d, J=8.3 Hz, 2H), 7.76 (br s, 1H), 7.74 (d, J=8.5 Hz, 2H), 7.73 (br s, 1H), 7.60 (d, J=8.5 Hz, 2H), 7.25 (br s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687639B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-85e758c5f54a4058a6e370adf52f4321 |
| Source note | uspto-grants-2010_03 |