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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359756Generated: October 29, 2026

Sulfuric Acid → HCID 178435494, compound

https://huagongshe.com/reaction/359756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
ReactantBilirubinHCID 5280352—
ReactantHCID 178435491HCID 178435491—
SolventMethanolHCID 887—
ProductHCID 178435494HCID 178435494—

Reaction Steps

The green filtrate was evaporated and purified by flash chromatography on Grade v neutral Alumina, eluting first with n-hexane to remove a fast running yellow band and then with dichloromethane to obtain the major blue/gray peak containing pheophytin-a. Treatment of pheophytin-a with 500 ml sulfuric acid in methanol for 12 hours at room temperature in the dark under nitrogen, was followed by dilution with dichloromethane. The reaction mixture was rinsed with water and then 10% aqueous sodium bicarbonate and the organic layer was dried, evaporated, and the residue recrystallized from dichloromethane/methanol to obtain 1.8 gm methyl pheophorbide-a. Methyl pheophorbide-a appears to be inactive in the in vivo tumorcidal activity assay when injected at a dose of 5 mg/kg; however, it is derivatized to the active compounds of the formula (4) above (pheophorbide derivatives) wherein R3 is a hydrophobic straight or branched chain saturated or unsaturated hydrocarbyl group containing 4-25 carbons and its hydrolyzed forms of formula (5) (the chlorin derivative), wherein R3 is as thus defined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002962
Source datasetuspto-grants-1991_03
ORD IDord-d18c1e5256a14d3898cf8aabb5f12517
Source noteuspto-grants-1991_03