| 查看: 1075 | 回复: 5 | ||||
caijacky0912木虫 (正式写手)
|
[求助]
求助埃索美拉唑钠的旋光值
|
|||
| 请教一下,谁能查到埃索美拉唑钠的旋光数据啊?只要有的都可以,谢谢! |
» 收录本帖的淘帖专辑推荐
新药研发 | 液相经验 |
» 猜你喜欢
一志愿北京协和医学院药理学292求调剂
已经有4人回复
一志愿北京协和药学专硕310 本科哈尔滨医科大学求调剂
已经有0人回复
药理学论文润色/翻译怎么收费?
已经有286人回复
2025年药学专业求调剂
已经有1人回复
[求助] 流式死活染 & 单细胞门控设置被质疑,如何优化并解释?
已经有1人回复
蛋白稳定性实验与功能实验不一致
已经有11人回复
第4年了,马上40了,可能我与国基确实无缘吧。。。
已经有12人回复
2026年申博药学专业
已经有1人回复
hardee
铁杆木虫 (知名作家)
此草有主~
- DRDEPI: 12
- 应助: 152 (高中生)
- 贵宾: 0.03
- 金币: 10928.3
- 散金: 5544
- 红花: 49
- 沙发: 40
- 帖子: 6865
- 在线: 2905.6小时
- 虫号: 891544
- 注册: 2009-11-02
- 性别: GG
- 专业: 药物化学
【答案】应助回帖
★ ★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
caijacky0912: 金币+5, ★★★很有帮助 2012-11-12 08:23:48
古可ぷ: 金币+2, 谢谢应助 2012-11-12 22:39:20
古可ぷ: 回帖置顶 2012-11-12 22:39:24
感谢参与,应助指数 +1
caijacky0912: 金币+5, ★★★很有帮助 2012-11-12 08:23:48
古可ぷ: 金币+2, 谢谢应助 2012-11-12 22:39:20
古可ぷ: 回帖置顶 2012-11-12 22:39:24
|
EP1515963 Example 4 Preparation of (-)-5-Methoxy-2-[[4-methoxy-3,5-dimethyl-2- pyridinyl) methyl]sulphinyl]-1H-benzimidazole Sodium Trihydrate Salt Sodium hydroxide flakes (4.5 grams) were added to methanol (50 ml) and stirred for 15-30 minutes. The mass was cooled to a temperature of 5-10°C, esomeprazole obtained as in Example 2 (25.0 grams), and methanol (100.0 ml) were added with stirring for 30-60 minutes. The solvent was expelled off completely from the reaction solution. Di-isopropyl ether (150 ml) was added to the residual mass and further stirred for 30-60 minutes. The mass was cooled to a temperature of 0-5°C and stirred for 30-60 minutes to separate the solid mass. The solid mass was filtered and dried at a temperature of 60-70°C under vacuum to afford optically pure Esomeprazole Sodium trihydrate salt. The characteristics of the product are as follows. Weight: 14.5 g. Chiral Purity: 99.53 Optical rotation: + 42° (c = 0.5% water) |

2楼2012-11-10 09:49:31
hardee
铁杆木虫 (知名作家)
此草有主~
- DRDEPI: 12
- 应助: 152 (高中生)
- 贵宾: 0.03
- 金币: 10928.3
- 散金: 5544
- 红花: 49
- 沙发: 40
- 帖子: 6865
- 在线: 2905.6小时
- 虫号: 891544
- 注册: 2009-11-02
- 性别: GG
- 专业: 药物化学
★ ★ ★ ★ ★
古可ぷ: 回帖置顶 2012-11-12 22:39:57
古可ぷ: 金币+5, 谢谢帮助,欢迎常来 2012-11-12 22:40:08
古可ぷ: 回帖置顶 2012-11-12 22:39:57
古可ぷ: 金币+5, 谢谢帮助,欢迎常来 2012-11-12 22:40:08
|
United States Patent Application 20070259921 POLYMORPHIC FORMS OF ESOMEPRAZOLE SODIUM 这篇专利也有埃索钠不同晶型的介绍,其中有比旋度,但未指明溶液浓度,应该是差不多的: Preparation of Crystalline Esomeprazole Sodium Form J 50 ml of methanol was taken into a round bottom flask and a mixture of 12.75 g sodium hydroxide and 11 ml of water was added to it and stirred for clear dissolution at 31° C. 110 g of esomeprazole was dissolved in 550 ml of methanol and the solution was added to the above methanolic sodium hydroxide solution. The mass was subjected to stirring at a temperature of 30° C. for 40 minutes, followed by the addition of 5.5 g of carbon with simultaneous stirring. The reaction mass was filtered through a Celite bed, and washed with 550 ml of methanol. The filtrate was subjected to distillation at a temperature of 30° C. under a vacuum of 200 torr. The residue was co-distilled with 1650 ml of acetone in three equal lots at 35° C. To the obtained residue, 220 ml of acetone was added and stirred for one hour. The separated solid was filtered and dried at 34° C. for 12 hours to afford 61.5 g of the title compound. Moisture content: 1.35% w/w. Specific optical rotation [α]D20=+43.220. Purity by HPLC 99.99%. Particle size distribution: D10 less than 3 μm, D50 less than 10 μm, D90 less than 30 μm. Bulk density: Before tapping: 0.428 g/ml. After tapping: 0.630 g/ml. EXAMPLE 2 Preparation of Crystalline Esomeprazole Sodium Form K 11.1 g of esomeprazole and 50 ml of methanol were taken in to a round bottom flask and stirred for 15 minutes. 1.0 g of carbon was added to the reaction mass and subjected to stirring for 30 minutes followed by filtration of the reaction mass through a Hyflow (flux calcined diatomaceous earth) bed. The filter bed was washed with 30 ml of methanol. The filtrate was transferred into a round bottom flask and stirred. 6 ml of aqueous sodium hydroxide was added to the filtrate and stirred for 40 minutes. Then the reaction mass was subjected to distillation under a vacuum of 100 torr at a temperature of 30° C. for 1 hour. The obtained residue was co-distilled with 150 ml of acetone in three equal lots under a vacuum of 200 torr and a temperature of 30° C. The residue obtained was taken into 200 ml of acetone and stirred for 30 minutes. The separated solid was filtered and washed with 20 ml of acetone. The wet solid was dried at a temperature of 34° C. for 7 hours to afford 54.5 g of the title compound. Moisture content: 8.87% w/w. Specific optical rotation: [α]D20=+41.32°. |
» 本帖已获得的红花(最新10朵)

4楼2012-11-12 12:44:06
caijacky0912
木虫 (正式写手)
- 应助: 14 (小学生)
- 金币: 2930.4
- 散金: 130
- 红花: 1
- 帖子: 565
- 在线: 200小时
- 虫号: 201676
- 注册: 2006-02-28
- 性别: GG
- 专业: 有机合成
3楼2012-11-12 11:55:04
caijacky0912
木虫 (正式写手)
- 应助: 14 (小学生)
- 金币: 2930.4
- 散金: 130
- 红花: 1
- 帖子: 565
- 在线: 200小时
- 虫号: 201676
- 注册: 2006-02-28
- 性别: GG
- 专业: 有机合成
5楼2012-11-12 21:11:00

6楼2014-10-16 19:56:29







回复此楼
caijacky0912