CN101302195A - 一种7-羟基-3,4-二氢喹诺酮的新合成方法 - Google Patents
一种7-羟基-3,4-二氢喹诺酮的新合成方法 Download PDFInfo
- Publication number
- CN101302195A CN101302195A CNA2008100625233A CN200810062523A CN101302195A CN 101302195 A CN101302195 A CN 101302195A CN A2008100625233 A CNA2008100625233 A CN A2008100625233A CN 200810062523 A CN200810062523 A CN 200810062523A CN 101302195 A CN101302195 A CN 101302195A
- Authority
- CN
- China
- Prior art keywords
- hydroxyl
- quinolone
- dihydro
- synthetic method
- hydroxyanilines
- 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
- 238000010189 synthetic method Methods 0.000 title claims description 16
- HLNPFTKVZWTEKP-UHFFFAOYSA-N 3,4-dihydroquinolin-7-ol Chemical class C1CC=NC2=CC(O)=CC=C21 HLNPFTKVZWTEKP-UHFFFAOYSA-N 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 claims abstract description 29
- LKLSFDWYIBUGNT-UHFFFAOYSA-N 7-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical compound C1CC(=O)NC2=CC(O)=CC=C21 LKLSFDWYIBUGNT-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000002904 solvent Substances 0.000 claims abstract description 13
- 239000003054 catalyst Substances 0.000 claims abstract description 11
- 239000011973 solid acid Substances 0.000 claims abstract description 9
- 238000005804 alkylation reaction Methods 0.000 claims abstract description 8
- 239000000706 filtrate Substances 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims abstract description 8
- 238000006555 catalytic reaction Methods 0.000 claims abstract description 3
- 238000010828 elution Methods 0.000 claims abstract description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 33
- 239000000460 chlorine Substances 0.000 claims description 23
- 229910052801 chlorine Inorganic materials 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- BUWPZNOVIHAWHW-UHFFFAOYSA-N 2,3-dihydro-1h-quinolin-4-one Chemical compound C1=CC=C2C(=O)CCNC2=C1 BUWPZNOVIHAWHW-UHFFFAOYSA-N 0.000 claims description 19
- 238000001816 cooling Methods 0.000 claims description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 16
- 239000002808 molecular sieve Substances 0.000 claims description 15
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 15
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical group [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 claims description 14
- 239000013078 crystal Substances 0.000 claims description 12
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 238000002425 crystallisation Methods 0.000 claims description 9
- 230000008025 crystallization Effects 0.000 claims description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 239000011230 binding agent Substances 0.000 claims description 7
- 239000003444 phase transfer catalyst Substances 0.000 claims description 7
- 125000003368 amide group Chemical group 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 238000001953 recrystallisation Methods 0.000 claims description 5
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical group [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- 238000005917 acylation reaction Methods 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 claims description 3
- 229910021536 Zeolite Inorganic materials 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical group O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 235000010755 mineral Nutrition 0.000 claims description 2
- 150000003242 quaternary ammonium salts Chemical group 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- 239000012467 final product Substances 0.000 claims 1
- 238000001308 synthesis method Methods 0.000 abstract 2
- PNLKLWHMPQKCEV-UHFFFAOYSA-N 3-chloro-n-(3-hydroxyphenyl)propanamide Chemical compound OC1=CC=CC(NC(=O)CCCl)=C1 PNLKLWHMPQKCEV-UHFFFAOYSA-N 0.000 abstract 1
- 238000006898 Intramolecular Friedel-Crafts reaction Methods 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 239000002912 waste gas Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical group [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 238000005516 engineering process Methods 0.000 description 5
- 239000012065 filter cake Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 230000003292 diminished effect Effects 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 239000007787 solid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- SWWQQSDRUYSMAR-UHFFFAOYSA-N 1-[(4-hydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol;hydrochloride Chemical group Cl.C1=CC(O)=CC=C1CC1C2=CC(O)=C(O)C=C2CCN1 SWWQQSDRUYSMAR-UHFFFAOYSA-N 0.000 description 1
- QFMJFXFXQAFGBO-UHFFFAOYSA-N 4-methoxy-2-nitroaniline Chemical compound COC1=CC=C(N)C([N+]([O-])=O)=C1 QFMJFXFXQAFGBO-UHFFFAOYSA-N 0.000 description 1
- KLTDQLIGNSBZPO-UHFFFAOYSA-N 4-methoxy-2-nitrobenzaldehyde Chemical compound COC1=CC=C(C=O)C([N+]([O-])=O)=C1 KLTDQLIGNSBZPO-UHFFFAOYSA-N 0.000 description 1
- CEUORZQYGODEFX-UHFFFAOYSA-N Aripirazole Chemical compound ClC1=CC=CC(N2CCN(CCCCOC=3C=C4NC(=O)CCC4=CC=3)CC2)=C1Cl CEUORZQYGODEFX-UHFFFAOYSA-N 0.000 description 1
- 229960004372 aripiprazole Drugs 0.000 description 1
- 239000003693 atypical antipsychotic agent Substances 0.000 description 1
- 229940127236 atypical antipsychotics Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- NCBZRJODKRCREW-UHFFFAOYSA-N m-anisidine Chemical compound COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Abstract
Description
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN2008100625233A CN101302195B (zh) | 2008-06-13 | 2008-06-13 | 一种7-羟基-3,4-二氢喹诺酮的合成方法 |
Applications Claiming Priority (1)
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CN2008100625233A CN101302195B (zh) | 2008-06-13 | 2008-06-13 | 一种7-羟基-3,4-二氢喹诺酮的合成方法 |
Publications (2)
Publication Number | Publication Date |
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CN101302195A true CN101302195A (zh) | 2008-11-12 |
CN101302195B CN101302195B (zh) | 2010-06-09 |
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CN2008100625233A Active CN101302195B (zh) | 2008-06-13 | 2008-06-13 | 一种7-羟基-3,4-二氢喹诺酮的合成方法 |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102850270A (zh) * | 2012-02-29 | 2013-01-02 | 池州方达科技有限公司 | 一锅法制备羟基取代-3,4-二氢-2(1h)-喹啉酮类化合物的方法 |
CN104356063A (zh) * | 2014-10-16 | 2015-02-18 | 华东师范大学 | 7-羟基-3,4-二氢-2-(1h)喹诺酮的制备方法 |
CN111285803A (zh) * | 2020-03-18 | 2020-06-16 | 湖南复瑞生物医药技术有限责任公司 | 一种6-羟基-3,4-二氢-2(1h)-喹诺酮的制备方法 |
-
2008
- 2008-06-13 CN CN2008100625233A patent/CN101302195B/zh active Active
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102850270A (zh) * | 2012-02-29 | 2013-01-02 | 池州方达科技有限公司 | 一锅法制备羟基取代-3,4-二氢-2(1h)-喹啉酮类化合物的方法 |
CN104356063A (zh) * | 2014-10-16 | 2015-02-18 | 华东师范大学 | 7-羟基-3,4-二氢-2-(1h)喹诺酮的制备方法 |
CN111285803A (zh) * | 2020-03-18 | 2020-06-16 | 湖南复瑞生物医药技术有限责任公司 | 一种6-羟基-3,4-二氢-2(1h)-喹诺酮的制备方法 |
CN111285803B (zh) * | 2020-03-18 | 2024-04-09 | 湖南复瑞生物医药技术有限责任公司 | 一种6-羟基-3,4-二氢-2(1h)-喹诺酮的制备方法 |
Also Published As
Publication number | Publication date |
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CN101302195B (zh) | 2010-06-09 |
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C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Zhejiang Tongfeng Pharmaceutical Chemical Co., Ltd. Assignor: Hangzhou Great Forest Biomedical Ltd. Contract record no.: 2011330000883 Denomination of invention: Novel synthetic method of 7-hydroxy-3,4-dihydroquinolines Granted publication date: 20100609 License type: Exclusive License Open date: 20081112 Record date: 20110704 |
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ASS | Succession or assignment of patent right |
Owner name: GU HAINING Free format text: FORMER OWNER: HANGZHOU GREAT FOREST BIOMEDICAL LTD. Effective date: 20130306 |
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C41 | Transfer of patent application or patent right or utility model | ||
COR | Change of bibliographic data |
Free format text: CORRECT: ADDRESS; FROM: 310028 HANGZHOU, ZHEJIANG PROVINCE TO: 311121 HANGZHOU, ZHEJIANG PROVINCE |
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TR01 | Transfer of patent right |
Effective date of registration: 20130306 Address after: Hangzhou District of Yuhang Zhejiang province 311121 Street warehouse before West No. 1378 Building 1 building F room 909-913 Patentee after: Gu Haining Address before: 603, room six, building 148, West Tianmu Road, 310028, Zhejiang, Hangzhou Patentee before: Hangzhou Great Forest Biomedical Ltd. |
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TR01 | Transfer of patent right |
Effective date of registration: 20180314 Address after: No. 15 Taizhou 317016 Zhejiang Province coastal Toumen Port District East Sixth Avenue Patentee after: ZHEJIANG BENLI CHEMICAL CO., LTD. Address before: Hangzhou District of Yuhang Zhejiang province 311121 Street warehouse before West No. 1378 Building 1 building F room 909-913 Patentee before: Gu Haining |
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TR01 | Transfer of patent right |