HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzoxazole → 2-(4-methylpiperazino)-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Product | 2-(4-methylpiperazino)-1,3-benzoxazole | HCID 3794539 | — |
Reaction Steps
To 3.08 g of 2-chlorobenzoxazole was added 200 ml of N-methylpiperazine under cooling with ice, followed by 2 hours of reaction at the same temperature. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was dissolved in 200 ml of ethyl acetate, washed with water, dehydrated with MgSO4 and then concentrated to dryness under a reduced pressure. The resulting residue was purified by a silica gel column chromatography (chloroform:methanol=20:1) to obtain 2.77 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05631257 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-88fe0893b27541d8bf0119e15a7e8d6b |
| Source note | uspto-grants-1997_05 |