HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propylphosphonic anhydride → Camptothecin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | N,N-dimethylpyridin-1-amine | HCID 6453552 | — |
| Reactant | HCID 86584209 | HCID 86584209 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Camptothecin | HCID 24360 | 8,851.2% |
Reaction Steps
A solution of 2.0 g (0.10 mmoles) of m-PEG20k acid, 60 mg (0.06 mmoles) of diaminopimelic camptothecin TFA salt, 0.064 mo (0.10 mmoles) of a 50% solution of 1-propanephosphonic acid cyclic anhydride in ethyl acetate and 25 mg (0.20 mmoles) of N-dimethylamino pyridine in 20 ml of dry dichloromethane was stirred at room temperature overnight followed by washing with 1% aqueous sodium bicarbonate and 0.1N HCl solution. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed by distillation in vacuo. The residue was crystallized from 2-propanol to yield 1.85 g (93% yield)of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251382B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-e17ba7ea6d124281af76da0b7571ec03 |
| Source note | uspto-grants-2001_06 |