HuagongsheHuagongshe Chemistry Print Report · For research reference only
Camptothecin → HCID 11024585, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Camptothecin | HCID 24360 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11024585 | HCID 11024585 | 97% |
Reaction Steps
In a 350 mL high pressure autoclave, 6 g (17.2 mmol) of camptothecin was suspended in 60 mL of acetic acid, and into which 1.2 g of stabilized nickel catalyst (N113) was added. After hydrogen substitution of the inside atmosphere, the suspension was heated at 110° C. under 2.0 MPa for 6 hours with stirring, whereat the starting material disappeared. The reaction liquid was cooled off to room temperature, filtered on 0.5 g of Celite and washed with 10 mL of acetic acid. An HPLC analysis of this solution confirmed that this Example could produce 1,2,6,7-tetrahydrocamptothecin at an yield of 97% (The diastereoisomeric ratio was 23:74).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299251B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-062c98caaf79487f92bc38deb059ba9c |
| Source note | uspto-grants-2012_10 |