Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | HCID 23155747 | HCID 23155747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23155692 | HCID 23155692 | 58.1% |
Reaction Steps
In a glass tube, 414 mg of 2-[4-(4-quinolin-2-ylpiperazin-1-yl)butyl]-3,1-benzoxazin-4-one as synthesized in above Step 7-15-B, 590 mg of isopropylamine and 5 ml of tetrahydrofuran were hermetically sealed and stirred for an hour at the exterior temperature of 80° C. Cooling the reaction mixture, the solvent was distilled off under reduced pressure, and the resulting residue was purified on silica gel column chromatography (dichloromethane:methanol=10:1) to provide 275 mg (58%) of N-isopropyl-2-[5-(4-quinolin-2-ylpiperazin-1-yl)pentanoylamino]benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07799775B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-a7e4d0c735a747978f28960af7214929 |
|---|
| Source note | uspto-grants-2010_09 |
|---|