HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonamide → HCID 10270136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | 6(5h)-Phenanthridinone, 2-amino- | HCID 270668 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10270136 | HCID 10270136 | 93% |
Reaction Steps
Prepared from 2-amino-6(5H)-phenanthridinone 3 and 4-methyl benzenesulfonamide according to General Procedure A. P-dioxane was used as solvent and the reaction was run at 40° C. for 30 hours. Purification of compound by crystallization in dioxane gave a brown solid (93% yield). mp 199-203° C. 1H-NMR (400 MHz, DMSO-d6), 10.20 (s, 1H), 8.30 (d, J=8.0 Hz, 1H), 8.15 (d, J=8.1 Hz, 1H), 7.95 (s, 1H), 7.88 (t, J=7.6, 1H), 7.65 (m, 3H), 7.33 (d, J=8.2 Hz, 2H), 7.19 (m, 2H). Anal. (C20H16N2O3S), C H N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723733B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-762ed160bbb541b29ddc2b9c4bedecfd |
| Source note | uspto-grants-2004_04 |