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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463993Generated: October 26, 2026

10-Aminocamptothecin → Hydroxycamptothecin

https://huagongshe.com/reaction/463993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant10-AminocamptothecinHCID 104986—
ReactantSodium NitriteHCID 23668193—
SolventSulfuric AcidHCID 1118—
SolventChloroformHCID 6212—
ProductHydroxycamptothecinHCID 9722666.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04545880
Source datasetuspto-grants-1985_10
ORD IDord-25e678f0cb5a4839b4ecf8ff355f4148
Source noteuspto-grants-1985_10