HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → HCID 20061408, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 20061231 | HCID 20061231 | — |
| Reactant | HCID 20061422 | HCID 20061422 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20061408 | HCID 20061408 | — |
Reaction Steps
6-(1-aziridinyl)-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione (compound 6) (0.45 g), 0.7 g of N-(2-hydroxyethyl)-3-(3-methoxy-4-nitrophenyl)propylamine and 50 mg of p-toluenesulfonic acid monohydrate was dissolved in 25 ml of acetonitrile and then the solvent was removed in vacuo. The resultant oil was allowed to react at 80° C. for 3 hours and then subjected to silica gel column chromatograph (chloroform/methanol=40/1, v/v) for purification; thereby 0.38 g of an oil, 1,3-dimethyl-6-{2-[N-(2-hydroxethyl)-3-(3-methoxy-4-nitrophenyl)propylamino]ethylamino}-2,4(1H,3H)-pyrimidinedione, was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008267 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-69284ebb6ddd49cd903a43a5546ad6f0 |
| Source note | uspto-grants-1991_04 |