HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 6-(3,4-Dimethoxyphenyl)-4-(4-mesylaminophenylamino)-2-methylpyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4-Aminophenylamino)-6-(3,4-dimethoxyphenyl)-2-methylpyrimidine | HCID 20152254 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 6-(3,4-Dimethoxyphenyl)-4-(4-mesylaminophenylamino)-2-methylpyrimidine | HCID 20152262 | — |
Reaction Steps
To a solution of 4-(4-aminophenylamino)-6-(3,4-dimethoxyphenyl)-2-methylpyrimidine (1.0 g) in 1,2-dichloroethane (20 ml) were added methanesulfonyl chloride (0.28 ml) and triethylamine (0.83 ml) and the mixture was refluxed for 3 hours. After cooled, chloroform (50 ml) was added thereto, and washed with water. The solution was dried over magnesium sulfate, evaporated, and chromatographed on silica gel eluting with chloroform to give 6-(3,4-dimethoxyphenyl)-4-(4-mesylaminophenylamino)-2-methylpyrimidine (0.45 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04725600 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-917a2479c3f9457d87255a214f0059bb |
| Source note | uspto-grants-1988_02 |