HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-[3-(4-Diphenylmethylpiperazine-1-yl)-2-hydroxypropylthio]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazine | HCID 10360175 | — |
| Reactant | 3056-03-9 | HCID 135755324 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-[3-(4-Diphenylmethylpiperazine-1-yl)-2-hydroxypropylthio]quinoline | HCID 15228135 | 20.3% |
Reaction Steps
In 10 ml of chloroform were dissolved 1.2 g of 4-(3-chloro-2-hydroxypropy)-1-diphenylmethylpiperazine prepared in Example 23-(b) and 220 mg of 5-mercaptoquinoline, and 311 mg of DBU was further added thereto. Afterward, the liquid was allowed to stand at room temperature for 12 days. The reaction liquid was poured into 20 ml of water and was then extracted twice with methylene chloride. The resultant organic layer was separated, then dried with an anhydrous Glauber's salt, and was distilled off under reduced pressure. The resultant residue was purified through a silica gel chromatograph (an AcOEt effluent solvent was used) in order to obtain 130 mg of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112817 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-a19f032918a74e80a5b574747c5bbf9f |
| Source note | uspto-grants-1992_05 |