CN103739525A - 一种取代苯磺酰氯的制备方法 - Google Patents
一种取代苯磺酰氯的制备方法 Download PDFInfo
- Publication number
- CN103739525A CN103739525A CN201310742587.9A CN201310742587A CN103739525A CN 103739525 A CN103739525 A CN 103739525A CN 201310742587 A CN201310742587 A CN 201310742587A CN 103739525 A CN103739525 A CN 103739525A
- Authority
- CN
- China
- Prior art keywords
- preparation
- reaction
- substituted phenylsulfonyl
- substituted
- phenylsulfonyl chloride
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical class ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 25
- 238000006243 chemical reaction Methods 0.000 claims abstract description 36
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 claims abstract description 30
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims abstract description 24
- 235000010288 sodium nitrite Nutrition 0.000 claims abstract description 15
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000002994 raw material Substances 0.000 claims abstract description 4
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract 5
- 239000012954 diazonium Substances 0.000 claims description 25
- 150000001989 diazonium salts Chemical class 0.000 claims description 24
- 239000000243 solution Substances 0.000 claims description 23
- 239000007864 aqueous solution Substances 0.000 claims description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 11
- 230000002378 acidificating effect Effects 0.000 claims description 10
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 238000000605 extraction Methods 0.000 claims description 6
- -1 nitro, methyl Chemical group 0.000 claims description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 6
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims description 5
- 150000001263 acyl chlorides Chemical class 0.000 claims description 5
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical group [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims description 5
- 229960003280 cupric chloride Drugs 0.000 claims description 5
- 229940045803 cuprous chloride Drugs 0.000 claims description 5
- 238000006193 diazotization reaction Methods 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000000284 extract Substances 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 3
- 238000010025 steaming Methods 0.000 claims description 3
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 235000015320 potassium carbonate Nutrition 0.000 claims description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- 235000017550 sodium carbonate Nutrition 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 1
- 239000002699 waste material Substances 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000000575 pesticide Substances 0.000 abstract description 2
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 18
- 150000001448 anilines Chemical class 0.000 description 8
- 230000035484 reaction time Effects 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical group ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000006575 electron-withdrawing group Chemical group 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229940124530 sulfonamide Drugs 0.000 description 3
- BLNVISNJTIRAHF-UHFFFAOYSA-N 4-chlorobenzamide Chemical compound NC(=O)C1=CC=C(Cl)C=C1 BLNVISNJTIRAHF-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 229940100389 Sulfonylurea Drugs 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 150000003456 sulfonamides Chemical class 0.000 description 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 2
- WTLNOANVTIKPEE-UHFFFAOYSA-N 2-acetyloxypropanoic acid Chemical compound OC(=O)C(C)OC(C)=O WTLNOANVTIKPEE-UHFFFAOYSA-N 0.000 description 1
- PBGKNXWGYQPUJK-UHFFFAOYSA-N 4-chloro-2-nitroaniline Chemical compound NC1=CC=C(Cl)C=C1[N+]([O-])=O PBGKNXWGYQPUJK-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- CKVRRALQQMYDMO-UHFFFAOYSA-N S(=O)(=O)(Cl)Cl.ClC1=CC=CC(=C1)[N+](=O)[O-] Chemical class S(=O)(=O)(Cl)Cl.ClC1=CC=CC(=C1)[N+](=O)[O-] CKVRRALQQMYDMO-UHFFFAOYSA-N 0.000 description 1
- YJLITVMNNGOLMO-UHFFFAOYSA-N [Cl].O(Cl)Cl.[S] Chemical compound [Cl].O(Cl)Cl.[S] YJLITVMNNGOLMO-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000007336 electrophilic substitution reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000019633 pungent taste Nutrition 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000005556 structure-activity relationship Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310742587.9A CN103739525B (zh) | 2013-12-30 | 2013-12-30 | 一种取代苯磺酰氯的制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310742587.9A CN103739525B (zh) | 2013-12-30 | 2013-12-30 | 一种取代苯磺酰氯的制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN103739525A true CN103739525A (zh) | 2014-04-23 |
CN103739525B CN103739525B (zh) | 2016-05-25 |
Family
ID=50496614
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201310742587.9A Active CN103739525B (zh) | 2013-12-30 | 2013-12-30 | 一种取代苯磺酰氯的制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103739525B (zh) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104961662A (zh) * | 2015-06-11 | 2015-10-07 | 湖南化工研究院有限公司 | 2-氟-6-三氟甲基苯磺酰氯的制备方法 |
CN105218413A (zh) * | 2015-08-12 | 2016-01-06 | 诚达药业股份有限公司 | 制备芳香磺酸类化合物的方法 |
CN106478464A (zh) * | 2016-08-30 | 2017-03-08 | 黄河三角洲京博化工研究院有限公司 | 一种2‑氟‑6‑三氟甲基苯磺酰氯的制备方法 |
CN106916087A (zh) * | 2015-12-25 | 2017-07-04 | 沈阳化工研究院有限公司 | 一种2-氟-6-三氟甲基苯磺酰氯的合成方法 |
CN107602566A (zh) * | 2017-09-26 | 2018-01-19 | 江苏省农用激素工程技术研究中心有限公司 | 双氟磺草胺中间体的合成方法 |
CN111574414A (zh) * | 2020-05-20 | 2020-08-25 | 上海毕得医药科技有限公司 | 一种4-溴-2-甲氧基苯磺酰氯的合成方法 |
CN112759536A (zh) * | 2019-11-05 | 2021-05-07 | 常州锐博生物科技有限公司 | 取代的苯磺酰氯的制备方法 |
CN113194949A (zh) * | 2018-12-18 | 2021-07-30 | 株式会社D.西医疗法研究所 | 异喹啉磺酰氯酸加成盐和其制造方法 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1443159A (zh) * | 2000-07-24 | 2003-09-17 | 拜尔作物科学有限公司 | 经取代的磺酰氨基甲基苯甲酸(衍生物)及其制备方法 |
CN1471532A (zh) * | 2000-09-26 | 2004-01-28 | �ݶ�ũ������˾ | 2-烷氧基-6-三氟甲基-N-([1,2,4]三唑并[1,5-c]嘧啶-2-基)苯磺酰胺的制备方法 |
WO2007023186A1 (en) * | 2005-08-26 | 2007-03-01 | Laboratoires Serono S.A. | Pyrazine derivatives and use as pi3k inhibitors |
CN102336689A (zh) * | 2011-08-29 | 2012-02-01 | 天津市筠凯化工科技有限公司 | 4-氯-3-(三氟甲基)苯磺酰氯的制备及其精制方法 |
CN102603582A (zh) * | 2012-02-28 | 2012-07-25 | 王继龙 | 一种合成邻甲酸甲酯苯磺酰胺的方法 |
CN103319489A (zh) * | 2013-07-12 | 2013-09-25 | 黑龙江大学 | 三唑并嘧啶磺酰胺化合物及合成方法和应用 |
CN103333120A (zh) * | 2013-06-22 | 2013-10-02 | 西南科技大学 | 甲基二磺隆的合成方法 |
-
2013
- 2013-12-30 CN CN201310742587.9A patent/CN103739525B/zh active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1443159A (zh) * | 2000-07-24 | 2003-09-17 | 拜尔作物科学有限公司 | 经取代的磺酰氨基甲基苯甲酸(衍生物)及其制备方法 |
CN1471532A (zh) * | 2000-09-26 | 2004-01-28 | �ݶ�ũ������˾ | 2-烷氧基-6-三氟甲基-N-([1,2,4]三唑并[1,5-c]嘧啶-2-基)苯磺酰胺的制备方法 |
WO2007023186A1 (en) * | 2005-08-26 | 2007-03-01 | Laboratoires Serono S.A. | Pyrazine derivatives and use as pi3k inhibitors |
CN102336689A (zh) * | 2011-08-29 | 2012-02-01 | 天津市筠凯化工科技有限公司 | 4-氯-3-(三氟甲基)苯磺酰氯的制备及其精制方法 |
CN102603582A (zh) * | 2012-02-28 | 2012-07-25 | 王继龙 | 一种合成邻甲酸甲酯苯磺酰胺的方法 |
CN103333120A (zh) * | 2013-06-22 | 2013-10-02 | 西南科技大学 | 甲基二磺隆的合成方法 |
CN103319489A (zh) * | 2013-07-12 | 2013-09-25 | 黑龙江大学 | 三唑并嘧啶磺酰胺化合物及合成方法和应用 |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104961662A (zh) * | 2015-06-11 | 2015-10-07 | 湖南化工研究院有限公司 | 2-氟-6-三氟甲基苯磺酰氯的制备方法 |
CN104961662B (zh) * | 2015-06-11 | 2017-05-03 | 湖南化工研究院有限公司 | 2‑氟‑6‑三氟甲基苯磺酰氯的制备方法 |
CN105218413A (zh) * | 2015-08-12 | 2016-01-06 | 诚达药业股份有限公司 | 制备芳香磺酸类化合物的方法 |
CN106916087B (zh) * | 2015-12-25 | 2018-08-14 | 沈阳化工研究院有限公司 | 一种2-氟-6-三氟甲基苯磺酰氯的合成方法 |
CN106916087A (zh) * | 2015-12-25 | 2017-07-04 | 沈阳化工研究院有限公司 | 一种2-氟-6-三氟甲基苯磺酰氯的合成方法 |
CN106478464B (zh) * | 2016-08-30 | 2018-06-05 | 黄河三角洲京博化工研究院有限公司 | 一种2-氟-6-三氟甲基苯磺酰氯的制备方法 |
CN106478464A (zh) * | 2016-08-30 | 2017-03-08 | 黄河三角洲京博化工研究院有限公司 | 一种2‑氟‑6‑三氟甲基苯磺酰氯的制备方法 |
CN107602566A (zh) * | 2017-09-26 | 2018-01-19 | 江苏省农用激素工程技术研究中心有限公司 | 双氟磺草胺中间体的合成方法 |
CN113194949A (zh) * | 2018-12-18 | 2021-07-30 | 株式会社D.西医疗法研究所 | 异喹啉磺酰氯酸加成盐和其制造方法 |
EP3900724A4 (en) * | 2018-12-18 | 2022-07-13 | D. Western Therapeutics Institute, Inc. | ISOQUINOLINE SULFONYL CHLORIDE ACID ADDITION SALT AND PROCESS FOR THE PREPARATION THEREOF |
US11535595B2 (en) | 2018-12-18 | 2022-12-27 | D. Western Therapeutics Institute, Inc. | Isoquinoline sulfonyl chloride acid addition salts and method of manufacture thereof |
CN113194949B (zh) * | 2018-12-18 | 2024-05-31 | 株式会社D.西医疗法研究所 | 异喹啉磺酰氯酸加成盐和其制造方法 |
CN112759536A (zh) * | 2019-11-05 | 2021-05-07 | 常州锐博生物科技有限公司 | 取代的苯磺酰氯的制备方法 |
CN111574414A (zh) * | 2020-05-20 | 2020-08-25 | 上海毕得医药科技有限公司 | 一种4-溴-2-甲氧基苯磺酰氯的合成方法 |
Also Published As
Publication number | Publication date |
---|---|
CN103739525B (zh) | 2016-05-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103739525A (zh) | 一种取代苯磺酰氯的制备方法 | |
RU96123762A (ru) | Способ получения d, l-метионина или его соли | |
CN105481744B (zh) | Co2/n2‑h2o2双重刺激响应型表面活性剂及其制备方法 | |
CN105348216A (zh) | 一种2-乙酰基噻唑的合成方法 | |
CN104945286A (zh) | 一种高纯度硫酸二酯的合成方法 | |
CN103601749B (zh) | 一种1-烷基吡唑-4-硼酸频哪醇酯的合成方法 | |
CN106243046A (zh) | 一种甲基二磺隆的制备方法 | |
CN103833593A (zh) | 一种n-(9-芴甲氧羰基)-o-叔丁基-l-酪氨酸的制备方法 | |
CN103193611B (zh) | 一种间三氟甲基苯乙酮的合成方法 | |
CN103910658B (zh) | 一种硫醚氧化成砜的方法 | |
CN107043322A (zh) | 一种2,4,6‑三氟苯甲醛的制备方法 | |
CN103588682B (zh) | 一种1,3-二氨基胍盐酸盐的制备方法 | |
CN106631941A (zh) | 一种2‑甲基‑3氯苯基甲硫醚的制备方法 | |
CN102634814A (zh) | 一种电化学合成肟的方法 | |
CN104072360A (zh) | 一种合成天然肉桂酸的方法 | |
CN102603485A (zh) | 制备2-甲基-3-苯基苯甲醇的方法 | |
CN103274944A (zh) | 氯甲酸甲酯的制备方法 | |
CN104119407A (zh) | 一种甲基-2,3,4-三氧-苄基-β-D-吡喃核糖苷的合成方法 | |
CN103923086B (zh) | 一种5-烷氧基-1,2,4-三唑[4,3-c]嘧啶-3(2H)-硫酮的制备方法 | |
CN104085869B (zh) | 采用咪唑磷酸二氢盐型离子液体合成纺锤形磷酸铋的方法 | |
CN107602407A (zh) | 一种2‑溴‑4‑氟乙酰苯胺的合成方法 | |
CN105237486A (zh) | 2-乙基-3,6-二甲基吡嗪的合成方法 | |
CN102146072B (zh) | 一种稻瘟灵的制备方法 | |
CN104774141A (zh) | 一种2-溴-9-芴酮的合成方法 | |
CN103351340A (zh) | 唑虫酰胺的新制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C53 | Correction of patent of invention or patent application | ||
CB03 | Change of inventor or designer information |
Inventor after: Li Ying Inventor after: Li Chengkun Inventor after: Zhang Jianlin Inventor after: Mou Qingping Inventor after: Wu Wenlei Inventor after: Yao Gang Inventor after: Hou Xiaofeng Inventor after: Cheng Lunan Inventor before: Li Ying Inventor before: Zhang Jianlin Inventor before: Mou Qingping Inventor before: Wu Wenlei Inventor before: Yao Gang Inventor before: Hou Xiaofeng Inventor before: Cheng Lunan |
|
COR | Change of bibliographic data |
Free format text: CORRECT: INVENTOR; FROM: LI YING ZHANG JIANLIN MOU QINGPING WU WENLEI YAO GANG HOU XIAOFENG CHENG LUNAN TO: LI YING LI CHENGKUN ZHANG JIANLIN MOU QINGPING WU WENLEI YAO GANG HOU XIAOFENG CHENG LUNAN |
|
ASS | Succession or assignment of patent right |
Owner name: CHAMBROAD AGROCHEMICAL TECHNOLOGY CO., LTD. Free format text: FORMER OWNER: YELLOW RIVER DELTA JINGBO CHEMICAL RESEARCH INSTITUTE CO., LTD. Effective date: 20141204 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20141204 Address after: 256500 Shandong city of Binzhou province Hu Zhen Boxing County Chen Jingbo Industrial Park Beijing Bo agricultural Polytron Technologies Inc Applicant after: JINGBO AGROCHEMICALS TECHNOLOGY Co.,Ltd. Address before: 256500 Boxing Economic Development Zone, Binzhou, Shandong Applicant before: CHAMBROAD CHEMICAL INDUSTRY RESEARCH INSTITUTE Co.,Ltd. |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: 256500 Boxing County Economic Development Zone, Binzhou, Shandong Patentee after: JINGBO AGROCHEMICALS TECHNOLOGY Co.,Ltd. Address before: 256500 Jingbo Agrochemical Technology Co., Ltd. of Jingbo Industrial Park, Chenhu Town, Boxing County, Binzhou City, Shandong Province Patentee before: JINGBO AGROCHEMICALS TECHNOLOGY Co.,Ltd. |
|
CP01 | Change in the name or title of a patent holder |
Address after: 256500 Boxing Economic Development Zone, Shandong, Binzhou Patentee after: Shandong Jingbo Agrochemical Technology Co.,Ltd. Address before: 256500 Boxing Economic Development Zone, Shandong, Binzhou Patentee before: JINGBO AGROCHEMICALS TECHNOLOGY Co.,Ltd. |
|
CP01 | Change in the name or title of a patent holder |