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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437029Generated: October 30, 2026

Sulfuric Acid → Vincristine

https://huagongshe.com/reaction/437029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium ChlorideHCID 5234—
ReactantSodium CarbonateHCID 10340—
ReactantVincristine SulfateHCID 249332—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductVincristineHCID 5978—

Reaction Steps

147.6 mg. of vincristine sulfate were slowly added to 877.1 mg. of cold 18 M sulfuric acid. After the addition had been completed, the reacton mixture was stirred (at ambient temperature) for one-half hour. 13 ml. of dry methanol were then added followed by 2.8193 g. of solid sodium carbonate. The resulting mixture was stirred for about 45 minutes. 40 ml. of saturated aqueous sodium chloride were then added, and the volume made up to 80 ml. with distilled water. The resulting aqueous solution was extracted four times with equal volumes of benzene. The benzene extracts were separated, combined, dried and the benzene removed by evaporation. A residue weighing 57.2 mg. was obtained containing a mixture of three anhydro derivatives shown as three separate spots on thin layer chromatography. The reaction mixture was separated by preparative thin layer chromatography on silica gel using methanol as the eluant. The preparative chromatogram was divided into three zones manually and the anhydro derivative in each zone removed from the silica adsorbent by two washes with an ethyl acetate-methylene dichloride solvent mixture followed by two washes with methanol. The mixture of three anhydro compounds obtained from vincristine by the above reaction was thus separated and purified. During the sulfuric acid treatment and subsequent isolation procedures, the C-4 acetyl group hydrolyzed and the resulting anhydro derivatives were all derivatives of C-4 desacetyl vincristine. Each of these compounds had the structure of Formula II above in which R is methoxy, R' is hydroxy and R" is formyl. 19.2 mg. of the 3',4'-isomer (Z is IIIa) were obtained having the following physical characteristics: Mass spectrograph: Molecular ion at 764, other peaks at 750, 736, 688, 676, 660, 554, 537, 494, 478, 336, 337, 279, 261, 247, 249, 219, 167, 149, 136, 120, 121, 111, 106 and a transmethylation peak at 778. (Partial) NMR spectrum (in deuterated chloroform) δ's (ppm) at 0.96, 3.58, 3.63, 3.74, 3.81, 3.87, and 5.41 (multiplet).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04029663
Source datasetuspto-grants-1977_06
ORD IDord-cbfcfdd152ba4fbb810807ee912c5d4f
Source noteuspto-grants-1977_06