HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633748Generated: October 31, 2026
N-(8-Amino-6-fluoro-5-methyl-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetamide → Exatecan intermediate 9
https://huagongshe.com/reaction/1633748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(8-Amino-6-fluoro-5-methyl-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetamide | HCID 10220585 | — |
| Reactant | (4S)-4-Ethyl-7,8-dihydro-4-hydroxy-1H-pyrano(3,4-f)indolizine-3,6,10(4H)-trione | HCID 10220900 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Exatecan intermediate 9 | HCID 12067229 | 91.4% |
Reaction Steps
To 2.00 g of 2-acetylamino-8-amino-6-fluoro-5-methyl-1-tetralone and 2.10 g of (4S)-4-ethyl-7,8-dihydro-4-hydroxy-1H-pyrano[3,4-f]indolizine-3,6,10(4H)-trione, 250 ml of toluene and then 0.1 g of pyridinium p-toluenesulfonate were added, followed by heating under reflux for 3 hours. The mixture was added with 0.1 g of pyridinium p-toluenesulfonate, followed by heating under reflux for 2.5 hours. The mixture was then added with 0.1 g of pyridinium p-toluenesulfonate, followed by heating under reflux for 38 hours. The reaction mixture was cooled. The solvent was then removed under reduced pressure. To a crystalline residue, acetone was added and the crystals so precipitated were collected by filtration, whereby 3.48 g of the title compound were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06504029B1 |
|---|
| Source dataset | uspto-grants-2003_01 |
|---|
| ORD ID | ord-725335c41bee44f49bf3ffa0c490a86e |
|---|
| Source note | uspto-grants-2003_01 |
|---|