The Polymorphism and Transformation of (3aRS, 4RS, 7RS, 7aSR)-2-(Tricyclo[3.3.1.13,7]decan-1-yl)-4,5,6,7-tetrahydro-4,7-eposyisoindoline-1,3-dione (SU2162)—A Novel Anticancer Compound
- 1 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 2 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 3 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 4 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 5 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 6 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 7 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 8 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
Abstract
Objective: To determine the transformation between two known crystal forms of the title compound (C 18 H 23 NO 3 , Mr = 301.37). Methods: To recrystallize or heat the crystals and determine the crystal form by testing the melting points. Results: Both the two known crystal forms of the title compound can be changed by dissolving into different organic solvents such as acetone and ethyl acetate. Crystal form I was not influenced by heating while crystal form II can be transformed to crystal form I through melting method. Conclusion: Organic solvents have significant influences on the two crystal forms of title compound. Crystal form I shows a better thermal stability than crystal form II .
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