Crystal forms of 2-aminoethyl sulfonic acid and preparation processes for crystal forms
A technology of aminoethanesulfonic acid and crystal form, applied in the field of crystal form and preparation of 2-aminoethanesulfonic acid, can solve the problems of no in-depth study of crystal form, low yield, high cost, etc., and achieve the effect of good druggability
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Embodiment 1
[0044] The preparation of embodiment 1 2-aminoethanesulfonic acid
[0045]According to the method disclosed in JP61282354A, 847.3 g of 2-aminoethanesulfonic acid was prepared and set aside.
Embodiment 22
[0046] The preparation of embodiment 22-aminoethanesulfonic acid crystal form I
[0047] Pick Example 1 50g of the prepared 2-aminoethanesulfonic acid was dissolved in 150ml of water, heated under reflux, decolorized with activated carbon for 30min, and suction filtered while it was hot. The filtrate was cooled to 5°C for crystallization, filtered with suction, washed with water, and dried under vacuum at 60-80°C. 31.4 g of crystalline form I of 2-aminoethanesulfonic acid were obtained.
Embodiment 3
[0048] Example 3 Preparation of 2-aminoethanesulfonic acid crystal form I
[0049] Pick Example 1 50g of the prepared 2-aminoethanesulfonic acid was dissolved in 100ml of water, heated under reflux, decolorized with activated carbon for 30min, and suction filtered while it was hot. The filtrate was cooled to 10°C for crystallization, filtered with suction, washed with water, and dried under vacuum at 60-80°C. 32.1 g of crystalline form I of 2-aminoethanesulfonic acid were obtained.
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