Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579985Generated: October 30, 2026

Acetic Acid → HCID 68131094, compound

https://huagongshe.com/reaction/1579985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitric AcidHCID 944—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-[(2H-[1,3]Dioxolo[4,5-g]isoquinolin-5-yl)amino]pentan-1-olHCID 21564761—
ProductHCID 68131094HCID 68131094—

Reaction Conditions

Temperature3 °C

Reaction Steps

A solution of 0.835 g. of 1-(5-hydroxypentyl)amino-6,7-methylenedioxyisoquinoline and 1 ml. of acetic acid is added dropwise to a stirred mixture of 1.32 ml. of acetic anhydride and 0.44 ml. of nitric acid at a temperature of minus 3°C. The reaction mixture is stirred for about 20 minutes at about minus 3°C., and then added to an excess of ice-cold aqueous ammonia solution and twice extracted with ethyl acetate. The combined organic extracts are dried, filtered and evaporated in vacuo to an oil which is redissolved in chloroform. The resulting solution is passed through silica gel to obtain 0.965 g. of an oil of the free base of the above title compound. This oil is dissolved in methylene chloride and 0.5 g. of maleic acid is added. The resulting solution is filtered, evaporated to a small volume and diethyl ether added to crystallize a material which is then recrystallized from methanol/diethyl ether to obtain 1-(5-hydroxypentyl)amino-6,7-methylenedioxyisoquinoline nitrate maleate, m.p. 138°-139.5°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932412
Source datasetuspto-grants-1976_01
ORD IDord-0b8a0112261347d3a5fa0157b4b88950
Source noteuspto-grants-1976_01