HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 18798244, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | o-(1-Piperazinyl)phenol | HCID 70530 | — |
| Reactant | HCID 18798239 | HCID 18798239 | — |
| Reactant | HCID 18798255 | HCID 18798255 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Tripropylamine | HCID 7616 | — |
| Product | HCID 18798244 | HCID 18798244 | — |
Reaction Steps
The 1,3,5-trimethyl-6-(3-chloropropylamino)-2,4(1H,3H)-pyrimidinedione prepared from 6.8 g (30 mmol) of 1,3,5-trimethyl-6-(3-hydroxypropylamino)-2,4(1H,3H)pyrimidinedione with thionyl chloride is refluxed for 15 h with 4.5 g (25 mmol) of 1-(2-hydroxyphenyl)piperazine in 140 ml of xylene and 20 ml of tripropylamine. The dark oil obtained after customary work-up is purified by column chromatography on silica gel using dichloromethane/methanol (1-10%). From the product fractions, the fumarate is precipitated from ethyl acetate/ethanol using fumaric acid, yield 5.9 g (47%), m.p. 203-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046329 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-ff53a2d14a544b2b875fa269376cbe39 |
| Source note | uspto-grants-2000_04 |