CN1302798A - Dl-苏式-对甲砜基苯基丝氨酸酯的拆分 - Google Patents
Dl-苏式-对甲砜基苯基丝氨酸酯的拆分 Download PDFInfo
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- 229940078547 methylserine Drugs 0.000 title 1
- BGFKIZNNZWWHAI-UHFFFAOYSA-M 2-oxo-2-(1h-pyrrol-3-yl)acetate Chemical compound [O-]C(=O)C(=O)C=1C=CNC=1 BGFKIZNNZWWHAI-UHFFFAOYSA-M 0.000 claims abstract description 21
- JKMPXGJJRMOELF-UHFFFAOYSA-N 1,3-thiazole-2,4,5-tricarboxylic acid Chemical compound OC(=O)C1=NC(C(O)=O)=C(C(O)=O)S1 JKMPXGJJRMOELF-UHFFFAOYSA-N 0.000 claims abstract description 19
- 230000003287 optical effect Effects 0.000 claims abstract description 7
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- SQUOCHQOQMZGQP-REOHCLBHSA-N raphanusamic acid Chemical compound OC(=O)[C@@H]1CSC(=S)N1 SQUOCHQOQMZGQP-REOHCLBHSA-N 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 229960003053 thiamphenicol Drugs 0.000 claims description 12
- 239000003960 organic solvent Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
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- 150000003863 ammonium salts Chemical class 0.000 claims description 3
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- 239000008096 xylene Substances 0.000 claims description 3
- 238000001556 precipitation Methods 0.000 claims description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000012044 organic layer Substances 0.000 claims 1
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- -1 ester ammonium salt Chemical class 0.000 description 8
- 125000004494 ethyl ester group Chemical group 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
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- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- NGPGDYLVALNKEG-UHFFFAOYSA-N azanium;azane;2,3,4-trihydroxy-4-oxobutanoate Chemical compound [NH4+].[NH4+].[O-]C(=O)C(O)C(O)C([O-])=O NGPGDYLVALNKEG-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012069 chiral reagent Substances 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- 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
- 229940079593 drug Drugs 0.000 description 1
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- JBIJRQVTPGGOHE-JTQLQIEISA-N ethyl (2s)-2-anilino-3-hydroxypropanoate Chemical compound CCOC(=O)[C@H](CO)NC1=CC=CC=C1 JBIJRQVTPGGOHE-JTQLQIEISA-N 0.000 description 1
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- OTVAEFIXJLOWRX-NXEZZACHSA-N thiamphenicol Chemical compound CS(=O)(=O)C1=CC=C([C@@H](O)[C@@H](CO)NC(=O)C(Cl)Cl)C=C1 OTVAEFIXJLOWRX-NXEZZACHSA-N 0.000 description 1
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- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
本发明属于DL-苏式-对甲砜基苯基丝氨酸酯的拆分技术。本发明采用的拆分试剂(R)-四氢噻唑-2-硫酮-4-羧酸[(R)TTCA]对DL-苏式-对甲砜基苯基丝氨酸酯进行拆分,合成(R)TTCA的原料易得,成本低,拆分过程简单。拆分得到的D-(+)-苏式-对甲砜基苯基丝氨酸酯及L-(-)-苏式-对甲砜基苯基丝氨酸酯的光学纯度可达98.0%,产率为85.0%以上。
Description
本发明是属于DL-苏式-对甲砜基苯基丝氨酸酯的拆分技术。
具有光学活性的D-(+)-苏式-对甲砜基苯基丝氨酸酯是合成抗菌活性和范围与氯霉素相似的甲砜霉素药物的重要中间体;因此,关于DL-苏式-对甲砜基苯基丝氨酸酯的拆分方法受到人们的重视。
DL-苏式-对甲砜基苯基丝氨酸酯的拆分一般是采用(+)-酒石酸[日本特许公开,昭50-137,952(1975);中国医药工业杂志,1979,10(5):1]为拆分试剂进行拆分。该拆分的方法是依据得到的非对映体(+)酒石酸铵盐,在甲醇中的溶解度不同,先后被析出。它的缺点是:(+)酒石酸:DL-氨基酯的摩尔比为1∶1,在甲醇中的分离操作比较麻烦,并影响产物的光学纯度和产率。
本发明用(R)-四氢噻唑-2-硫酮-4-羧酸[简称(R)TTCA]为拆分试剂对DL-苏式-对甲砜基苯基丝氨酸酯进行拆分。其特点是:(R)TTCA是一种手性试剂首次用在DL-苏式-对甲砜基苯基丝氨酸酯的拆分上;其合成方法简单,原料易得,成本低,反应的摩尔比为1∶2;操作简单,容易分离。
拆分得到的D-(+)-苏式-对甲砜基苯基丝氨酸酯及L-(-)-苏式-对甲砜基苯基丝氨酸酯产率为85.0%以上,光学纯度达98.0%以上。
本发明是将(R)TTCA溶于有机溶剂乙醇或甲醇、氯仿、乙酸乙酯、丙酮、二甲苯等,在20~120℃下反应,一般反应温度在40~80℃下,滴加到相应的有机溶剂溶解的DL-苏式-对甲砜基苯基丝氨酸酯溶液中,滴加后继续反应10~90分钟,一般继续反应控制在30~50分钟,生成大量白色沉淀,过滤出白色固体为(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸酯的铵盐,产率达98.0%以上。
滤液用无水Na2SO4干燥,蒸出有机溶剂,得到光学活性的L-(-)-苏式-对甲砜基苯基丝氨酸酯,产率达90.0%以上,光学纯度98.0%以上。
将(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸酯铵盐以水溶解,以NH4OH溶液中和至pH=7~8,有大量白色沉淀析出,滤出沉淀,滤饼用少量水洗三次,得D-(+)-苏式-对甲砜基苯基丝氨酸酯,产率达85%以上,光学纯度达98.0%以上。
实施例1:将0.1640g(1mmol)(R)TTCA溶于10mL乙醇中,50℃搅拌下滴加入10mL溶有0.5747g(2mmol)DL-苏式-对甲砜基苯基丝氨酸乙酯的乙醇中,滴加之后继续反应30分钟,体系产生大量白色沉淀,过滤得白色固体为(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐,产率98.20%,[a]20 D-46.24℃(c 0.20,H2O),m.p.159~160℃。
滤液以无水Na2SO4干燥,蒸出乙醇,得L-(-)-苏式-对甲砜基苯基丝氨酸乙酯,产率94.60%,[a]20 D-15.10℃(c 0.20,1,4-二氧六环),m.p.129~131℃。
将(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐用水溶解,以浓NH4OH中和到pH=7~8,滤出白色固体即为产品D-(+)-苏式-对甲砜基苯基丝氨酸乙酯,产率85%以上,[a]20 D+15.21°(c 0.25,1,4-二氧六环),m.p 129~131℃。
实施例2:改变溶液乙醇为甲醇,其它配方、反应条件完全与实施例1相同,结果(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐,产率98.40%,得L-(-)-苏式-对甲砜基苯基丝氨酸乙酯,产率98.00%。
实施例3:改变溶液乙醇为氯仿,其它配方、反应条件完全与实施例1相同,结果(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐,产率98.30%,得L-(-)-苏式-对甲砜基苯基丝氨酸乙酯,产率97.00%。
实施例4:改变溶液乙醇为乙酸乙酯,其它配方、反应条件完全与实施例1相同,结果(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐,产率98.30%,得L-(-)-苏式-对甲砜基苯基丝氨酸乙酯,产率96.10%。
实施例5:改变溶液乙醇为丙酮,其它配方、反应条件完全与实施例1相同,结果(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐,产率98.25%,得L-(-)-苏式-对甲砜基苯基丝氨酸乙酯,产率95.00%。
实施例6:改变溶液乙醇为二甲苯,其它配方、反应条件完全与实施例1相同,结果(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸乙酯铵盐,产率98.20%,得L-(-)-苏式-对甲砜基苯基丝氨酸乙酯,产率94.10%。
Claims (2)
1、一种DL-苏式-对甲砜基苯基丝氨酸酯的拆分方法,其特征在于:用拆分试剂(R)-四氢噻唑-2-硫酮-4-羧酸[(R)TTCA]对DL-苏式-对甲砜基苯基丝氨酸酯进行拆分,(R)TTCA与DL-苏式-对甲砜基苯基丝氨酸酯的反应摩尔比为1∶2;反应温度为20~120℃;反应介质为有机溶剂:CH3OH或C2H5OH、CHCl3、CH3COOC2H5、CH3COCH3、二甲苯等;反应10~90分钟,生成大量白色沉淀,过滤出白色固体为(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸酯的铵盐;滤液用饱和NaCl水溶液洗,有机层用无水Na2SO4干燥,蒸出有机溶剂得到光学活性的L-(-)-苏式-对甲砜基苯基丝氨酸酯,产率可达90.0%以上,光学纯度98.0%以上;(R)TTCA·D-(+)-苏式-对甲砜基苯基丝氨酸酯的铵盐以水溶解,用NH4OH溶液调至pH=7~8滤出白色固体为产品D-(+)-苏式-对甲砜基苯基丝氨酸酯,产率85%以上,光学纯度98.0%以上。
2、如权利要求1所述的DL-苏式-对甲砜基苯基丝氨酸酯的拆分方法,其特征在于反应温度为40~80℃,反应时间为30~50分钟。
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104326901A (zh) * | 2014-10-16 | 2015-02-04 | 安徽扬子化工有限公司 | D-乙酯生产中回收和套用l-(+)-酒石酸的方法 |
| CN104355990A (zh) * | 2014-10-16 | 2015-02-18 | 安徽扬子化工有限公司 | 一种d-乙酯生产中回收和套用l-(+)-酒石酸的方法 |
| CN107417585A (zh) * | 2017-06-22 | 2017-12-01 | 浙江海翔川南药业有限公司 | 一种药物中间体的合成方法 |
| CN108642120A (zh) * | 2018-05-23 | 2018-10-12 | 山东汉兴医药科技有限公司 | 一种d-对甲砜基苯丝氨酸乙酯的制备方法 |
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| JPH05202471A (ja) * | 1992-01-28 | 1993-08-10 | Fujitsu Ltd | マグネトロンスパッタリング装置 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104326901A (zh) * | 2014-10-16 | 2015-02-04 | 安徽扬子化工有限公司 | D-乙酯生产中回收和套用l-(+)-酒石酸的方法 |
| CN104355990A (zh) * | 2014-10-16 | 2015-02-18 | 安徽扬子化工有限公司 | 一种d-乙酯生产中回收和套用l-(+)-酒石酸的方法 |
| CN107417585A (zh) * | 2017-06-22 | 2017-12-01 | 浙江海翔川南药业有限公司 | 一种药物中间体的合成方法 |
| CN108642120A (zh) * | 2018-05-23 | 2018-10-12 | 山东汉兴医药科技有限公司 | 一种d-对甲砜基苯丝氨酸乙酯的制备方法 |
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