HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 178492142, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | p-sulfoaminoaniline | HCID 10997776 | — |
| Reactant | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Reactant | HCID 178516237 | HCID 178516237 | — |
| Product | HCID 178492142 | HCID 178492142 | — |
| Product | HCID 178516435 | HCID 178516435 | — |
Reaction Steps
2,3-dihydroxypyridine (0.0021 Mol), p-methoxyaniline (0.0027 mol), p-sulfoaminoaniline (0.0027 mol) and NaIO3 (0.0009 mol) were dissolved in 160 ml of water/acetone (80:1, v/v) solvent. The reaction mixture was stirred for 4 hours, and maintained still overnight. 5-p-methoxyphenylamino-6-(p-sulfoaminophenylamino)-2,3-pyridindione and 6-p-methoxyphenylamino-5-(p-sulfoaminophenylamino)-2,3-pyridindione were purified by passing the filtered reaction mixture through a silica gel column (100-200 mesh). The yield was 12%-16%. 5,6-di(p-methoxyphenylamino)-2,3-pyridindione and 5,6-di(p-sulfoaminophenylamino)-2,3-pyridindione can also be obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547713B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-5cc4ca10819a4ad0a52143bdb44fa761 |
| Source note | uspto-grants-2009_06 |