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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050822Generated: October 30, 2026

Phosphoric Acid → HCID 67340740, compound

https://huagongshe.com/reaction/1050822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 67341286HCID 67341286—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67340740HCID 67340740—

Reaction Conditions

Temperature60 °C

Reaction Steps

Analogously as described for Example 35 acidic acid (2R,4aR,10bR)-6-(6-cyano-pyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a,10b-hexahydro-phenanthridin-2-yl ester (compound 172) is converted in a first step into the corresponding imino ester 5-((2R,4aR,10bR)-9-ethoxy-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydro-phenanthridin-6-yl)-pyridine-2-carboximidic acid methyl ester. In a second step, 443 mg (1.08 mmol) of 5-((2R,4aR,10bR)-9-ethoxy-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydro-phenanthridin-6-yl)-pyridine-2-carboximidic acid methyl ester are dissolved in 3 ml of THF. A solution of 51 mg (2.16 mmol) LiOH.H2O is added and the solution stirred at 60° C. for 18 hrs. The pH is adjusted to 5 using phosphoric acid and Disodiumhydrogenphosphate. The solvent is removed and the solid residue extracted with chloroform/methanol. After filtering off and re-moving the volatiles 350 mg (82%) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09387205B2
Source datasetuspto-grants-2016_07
ORD IDord-2177ae469902416e98a519a1e3e58e7c
Source noteuspto-grants-2016_07