HuagongsheHuagongshe Chemistry Print Report · For research reference only
M-Phenylenediamine → N1-(4-(phenylthio)pyrimidin-2-yl)benzene-1,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | M-Phenylenediamine | HCID 7935 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-4-(phenylthio)pyrimidine | HCID 21995205 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N1-(4-(phenylthio)pyrimidin-2-yl)benzene-1,3-diamine | HCID 68746426 | 42% |
Reaction Steps
To a stirred mixture of 2-chloro-4-(phenylthio)pyrimidine (300 mg, 1.35 mmol) and diisopropylethylamine (0.35 mL, 2.02 mmol) in 2-ethoxyethanol (2 mL), was added 1,3-phenylenediamine (291 mg, 2.70 mmol) in one portion. The whole was heated under reflux for 20 hours. The mixture was cooled to room temperature, diluted with ethyl acetate (20 mL), washed with water and brine. The organic solution was dried (Na2SO4), concentrated in vacuo. The residue was flash chromatographed on silica gel using ethyl acetate:petroleum ether (20:80→50:50) as eluant to give the product (167 mg, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040549B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-a2fff81be1694ddd90762a623013500b |
| Source note | uspto-grants-2015_05 |