CN110642765A - 一种d-对甲砜基苯丝氨酸乙酯的合成方法 - Google Patents
一种d-对甲砜基苯丝氨酸乙酯的合成方法 Download PDFInfo
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 125000004494 ethyl ester group Chemical group 0.000 claims abstract description 12
- 238000001914 filtration Methods 0.000 claims abstract description 12
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- 229910000365 copper sulfate Inorganic materials 0.000 claims abstract description 6
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims abstract description 6
- PSVPUHBSBYJSMQ-UHFFFAOYSA-N 4-methylsulfonylbenzaldehyde Chemical compound CS(=O)(=O)C1=CC=C(C=O)C=C1 PSVPUHBSBYJSMQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000004471 Glycine Substances 0.000 claims abstract description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 5
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000003513 alkali Substances 0.000 claims abstract description 3
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 3
- 229910001431 copper ion Inorganic materials 0.000 claims abstract description 3
- 238000005886 esterification reaction Methods 0.000 claims abstract description 3
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical class [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000007787 solid Substances 0.000 claims description 10
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 6
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 6
- 150000001879 copper Chemical class 0.000 claims description 6
- 239000012065 filter cake Substances 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 6
- 238000010992 reflux Methods 0.000 claims description 6
- 238000000967 suction filtration Methods 0.000 claims description 6
- 235000019441 ethanol Nutrition 0.000 claims description 4
- 230000006340 racemization Effects 0.000 claims description 4
- 230000032050 esterification Effects 0.000 claims description 2
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 2
- 239000012452 mother liquor Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000004321 preservation Methods 0.000 claims description 2
- 238000010189 synthetic method Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 8
- 239000010413 mother solution Substances 0.000 abstract description 5
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- 238000002425 crystallisation Methods 0.000 abstract description 2
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- 238000003912 environmental pollution Methods 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 230000002194 synthesizing effect Effects 0.000 abstract description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- JENNGODPHICNJP-FVGYRXGTSA-N [Cu].CS(=O)(=O)C1=CC=C(C=C1)N[C@@H](CO)C(=O)O Chemical compound [Cu].CS(=O)(=O)C1=CC=C(C=C1)N[C@@H](CO)C(=O)O JENNGODPHICNJP-FVGYRXGTSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
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- AYIRNRDRBQJXIF-NXEZZACHSA-N (-)-Florfenicol Chemical compound CS(=O)(=O)C1=CC=C([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)C=C1 AYIRNRDRBQJXIF-NXEZZACHSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
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- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/04—Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
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Abstract
本发明公开了一种D‑对甲砜基苯丝氨酸乙酯的合成方法,包括以下步骤:以对甲砜基苯甲醛、硫酸铜和甘氨酸为主要原料制备对甲砜基苯丝氨酸铜,在酯化反应釜中,再加入无水乙醇,浓硫酸,加热反应,趁热过滤掉硫酸铜,降温结晶,过滤得DL对甲砜基苯丝氨酸乙酯硫酸盐,将DL对甲砜基苯丝氨酸乙酯硫酸盐溶入水中,用饱和硫化钠溶液去除铜离子,母液加碱游离得DL对甲砜基苯丝氨酸乙酯,加入拆分剂拆分得到产物;本发明工艺简单、收率高、成本低、环境污染小,适合企业化生产。
Description
技术领域
本发明属于化合物合成领域,具体是一种D-对甲砜基苯丝氨酸乙酯的合成方法。
背景技术
氟苯尼考是新一代氯霉素类动物专用广谱抗生素,在临床医疗及农业上有着广泛的用途,近年来,人们对其需求量正在逐年增加。而D-对甲砜基苯丝氨酸乙酯是合成氟苯尼考的重要原材料,传统合成工艺复杂,而且成本相对较高,收率低,因此,研发一种工艺简单、收率高、成本低的D-对甲砜基苯丝氨酸乙酯的合成方法势在必行。
发明内容
本发明的目的就是提供一种工艺简单、收率高、成本低的D-对甲砜基苯丝氨酸乙酯的合成方法。
本发明包括以下步骤:
(1)铜盐制备:将硫酸铜溶于水中,加入甘氨酸,对甲砜基苯甲醛,用氨水调节pH=6~9,保温反应16-25小时,反应结束后降温抽滤得到铜盐。
(2)酯化:将铜盐、无水乙醇加入反应釜,滴加浓硫酸,回流反应,趁热滤除无机盐,降温结晶抽滤,滤饼用水溶解,加饱和硫化钠溶液去除铜离子,加碱游离得到DL-对甲砜基苯丝氨酸乙酯。
(3)拆分:将DL-对甲砜基苯丝氨酸乙酯溶于乙醇,加入拆分剂拆分,将固体滤出,得到产物,母液进行消旋套用。
本发明有益效果为:本发明工艺简单、收率高、成本低、环境污染小,适合企业化生产。
具体实施方式
实施例1
在500ml反应瓶中,投入34g 硫酸铜,250ml纯化水,搅拌溶解,加入19g甘氨酸,42g对甲砜基苯甲醛,氨水调节pH=9,水溶控温50℃反应22小时,抽滤,滤饼溶于300ml无水乙醇,滴加浓硫酸40g,回流2.5小时,热过滤,收集母液,降温结晶,抽滤,将滤饼溶于水中,氨水调节pH=9,析出固体,过滤干燥得到消旋酯,将消旋酯溶于3倍乙醇,加入L-酒石酸,回流2.5小时,得到固体即为产物,母液消旋套用,固体干燥,得产品20.1g,收率42.3%。
实施例2
在500ml反应瓶中,投入34g 硫酸铜,250ml纯化水,搅拌溶解,加入19g甘氨酸,42g对甲砜基苯甲醛,氨水调节pH=8,水溶控温50℃反应21小时,抽滤,滤饼溶于300ml无水乙醇,滴加浓硫酸40g,回流3小时,热过滤,收集母液,降温结晶,抽滤,将滤饼溶于水中,氨水调节pH=8,析出固体,过滤干燥得到消旋酯,将消旋酯溶于3倍乙醇,加入L-酒石酸,回流2.5小时,得到固体即为产物,母液消旋套用,固体干燥,得产品19.8g,收率41.7%。
Claims (1)
1.一种D-对甲砜基苯丝氨酸乙酯的合成方法,其特征在于包括以下步骤:
(1)铜盐制备:将硫酸铜溶于水中,加入甘氨酸,对甲砜基苯甲醛,用氨水调节pH=6~9,保温反应16-25小时,反应结束后降温抽滤得到铜盐;
(2)酯化:将铜盐、无水乙醇加入反应釜,滴加浓硫酸,回流反应,趁热滤除无机盐,降温结晶抽滤,滤饼用水溶解,加饱和硫化钠溶液去除铜离子,加碱游离得到DL-对甲砜基苯丝氨酸乙酯;
(3)拆分:将DL-对甲砜基苯丝氨酸乙酯溶于乙醇,加入拆分剂拆分,将固体滤出,得到产物,母液进行消旋套用。
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Cited By (2)
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CN112479946A (zh) * | 2020-11-27 | 2021-03-12 | 普洛药业股份有限公司 | 一种高立体选择性制备d-对甲砜基苯丝氨酸乙酯的方法 |
CN115677546A (zh) * | 2022-12-30 | 2023-02-03 | 山东国邦药业有限公司 | 一种d-对甲砜基苯丝氨酸乙酯的手性合成方法 |
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Publication number | Priority date | Publication date | Assignee | Title |
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CN112479946A (zh) * | 2020-11-27 | 2021-03-12 | 普洛药业股份有限公司 | 一种高立体选择性制备d-对甲砜基苯丝氨酸乙酯的方法 |
CN115677546A (zh) * | 2022-12-30 | 2023-02-03 | 山东国邦药业有限公司 | 一种d-对甲砜基苯丝氨酸乙酯的手性合成方法 |
CN115677546B (zh) * | 2022-12-30 | 2023-03-07 | 山东国邦药业有限公司 | 一种d-对甲砜基苯丝氨酸乙酯的手性合成方法 |
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