HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → 6-[3-(N-methyl-N-benzylamino)-2-hydroxypropoxy]carbostyril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | 6-(Oxiran-2-ylmethoxy)quinolin-2(1H)-one | HCID 15015523 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-[3-(N-methyl-N-benzylamino)-2-hydroxypropoxy]carbostyril | HCID 10359775 | 72.9% |
Reaction Steps
To a solution of N-methylbenzylamine (21 g) in methanol (50 ml), a solution of 6-(2,3-epoxypropoxy)carbostyril (4.4 g) in methanol (70 ml) is added dropwise over a period of 30 minutes under refluxing with heat. After the addition, the mixture is further heated with refluxing for 2 hours. The reaction mixture is concentrated under reduced pressure, and the resulting residue is purified by silica gel column chromatography (solvent; methanol:chloroform=1:100-1:25) and recrystallized from ethanol to give 6-[3-(N-methyl-N-benzylamino)-2-hydroxypropoxy]carbostyril (5 g), as white powder, m.p. 129°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05266577 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-b6fe6136f3904c6b92192de5639876f4 |
| Source note | uspto-grants-1993_11 |