HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463993Generated: October 26, 2026
10-Aminocamptothecin → Hydroxycamptothecin
https://huagongshe.com/reaction/463993
Participants
| Role | Name | HCID | Charge |
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| Reactant | 10-Aminocamptothecin | HCID 104986 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Hydroxycamptothecin | HCID 97226 | 66.5% |
Reaction Steps
10-Aminocamptothecin (50 mg, 0.138 m-mol) is dissolved in a 10% aqueous solution of sulfuric acid (5 ml). To this solution in a salted ice bath is added dropwise slowly an aqueous solution of sodium nitrite (9.5 mg, 0.138 m-mol) with stirring. After the addition of sodium nitrite, the mixture is further stirred for 10 minutes in a salted ice bath. To the reaction mixture is added conc. sulfuric acid (1 ml), and the whole is boiled under reflux for 2 hours. The reaction mixture is diluted with ice water (200 ml) and chloroform (200 ml) is added. The mixture is shaken in a separating funnel and the resultant emulsion is filtered through celite. The chloroform phase containing camptothecin formed as by-product by side reactions is dried over magnesium sulfate, filtered and evaporated until dryness under reduced pressure whereby camptothecin (8 mg) is recovered. On the other hand, a solid on the celite, which is insoluble in chloroform-water, is taken up in 20% MeOH-CHCl3 (200 ml) and the solution is evaporated until dryness under reduced pressure whereby 28 mg (yield: 66.5% ) of the title compound is obtained as light yellow crystals. M.P. (with decomp.) 270°-272° C. (from pyridine-methanol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04545880 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-25e678f0cb5a4839b4ecf8ff355f4148 |
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| Source note | uspto-grants-1985_10 |
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