Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63778Generated: October 25, 2026

Phosphoric Acid → HCID 131737206, compound

https://huagongshe.com/reaction/63778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
Reactant5-Chloro-2-methyl-2,3,3a,12b-tetrahydrodibenzo(2,3:6,7)oxepino(4,5-c)pyrroleHCID 9903970—
SolventEthanolHCID 702—
ProductHCID 131737206HCID 131737206105.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

0.71 Kg of crude asenapine base (2.48 moles) and 6.7 L of ethanol are loaded into a reactor and dissolved by heating at 50° C. An 85% solution of phosphoric acid (0.17 L, 2.48 moles) in ethanol (1.0 L) is dripped into the solution of asenapine base at 50° C. in 10 minutes. The solution is stirred for 30 minutes at 50° C. The solution is cooled to 25° C. in approx. 2 hours. The solution is left under stirring at 25° C. for 2 hours. The product is isolated by filtration, washing with ethanol (1.1 L). The product is dried under vacuum at 25° C. for 20 hours. 1 Kg of asenapine phosphate is obtained (yield=94.0%). Purity >99.5% (HPLC). The IR spectrum, the DSC thermogram and the XRPD spectrum of asenapine phosphate are shown in FIGS. 1, 2 and 3 respectively. Table 1 shows the Bragg 2-theta angles (2θ), interplanar distances d and the relative intensities expressed as a percentage of the most intense diffraction peak. Table 3 shows the improvement in the quality of the product, expressed as HPLC area %, obtained in the conversion from asenapine base to asenapine phosphate. In Table 3, RRT indicates the relative retention time of the impurities present in the product obtained, compared with the retention time of asenapine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447109B2
Source datasetuspto-grants-2016_09
ORD IDord-f4ad76cc9b4f4d50807b9df10fec7b62
Source noteuspto-grants-2016_09