首页> 外国专利> DERIVATIVES OF 1,2,3,4-TETRAHYDROBENZOTHIENO 2,3-CPYRIDINE AND OF 1,2,3,4-TETRAHYDRO-5H-BENZOTHIENO2,3-CAZEPINE

DERIVATIVES OF 1,2,3,4-TETRAHYDROBENZOTHIENO 2,3-CPYRIDINE AND OF 1,2,3,4-TETRAHYDRO-5H-BENZOTHIENO2,3-CAZEPINE

机译:1,2,3,4-四氢联苯并噻吩并[2,3-C]吡啶和1,2,3,4-四氢-5H-苯并噻吩并[2,3-C]氮杂哌啶的衍生物

摘要

1,210,106. 1,2,3,4-Tetrahydrobenzothieno[2,3- c]pyridine and 1,2,3,4 - tetrahydro - 5H - benzothiene[2,3-c]azepine derivatives. COLGATEPALMOLIVE CO. 6 March, 1968 [8 March, 1967 (2); 6 Feb., 1968 (2)], No. 10892/68. Heading C2C. Novel 1,2,3,4 - tetrahydrobenzothieno[2,3 - c] pyridine and 1,2,3,4 - tetrahydro - 5H - benzothieno[2,3-c]azepine derivatives of the general formula wherein A and A 1 are the same or different and are hydrogen or halogen atoms or hydroxy, nitro, C 1-4 alkyl, C 1-3 alkoxy or trifluoromethyl groups; m is 1 or 2; R is a hydrogen atom or a C 1-4 alkyl, C 7-11 aralkyl, -(CH 2 ) n OH (in which n is from 2 to 6), B-Am, -COOR 1 , -COBAm or amidino group, in which B is a single chemical bond or a C 1-6 alkylene group; R 1 is a C 1-4 alkyl, di-(C 1-4 alkyl)amino-C 1-4 alkyl, hydroxy- C 1-4 alkyl, C 3-6 alkenyl, C 7-11 aralkyl, C 3-7 cycloalkyl or C 3-7 cycloalkyl-C 1-4 alkyl group; and Am is (a) -NR 2 R 3 in which R 2 and R 3 are the same or different and are hydrogen atoms or C 1-4 alkyl, di-(C 1-4 alkyl)-amino-C 1-4 alkyl, hydroxy-C 1-4 alkyl, C 3-6 alkenyl, C 3-7 cycloalkyl or C 3-7 cycloalkyl-C 1-4 alkyl groups; (b) a morpholino, pyrrolidino, piperidino, N-C 1-4 alkyl - piperazino, N - (phenyl - C 1-4 alkyl). piperazino or N-(hydroxy C 1-4 alkyl)-piperazino group; or (c) a piperidyl or pyrrolidyl radical bonded through a nuclear carbon atom to B; and X 1 and X 2 are the same or different and are hydrogen atoms or C 1-4 alkyl, phenyl, halo- or alkoxy-substituted phenyl, C 7-11 aralkyl, piperidyl, pyridyl, furyl, pyrryl, pyrrolidyl or B-Am groups, provided that X 2 is not a hydrogen atom when X 1 and R are both hydrogen atoms; and pharmaceutically acceptable acid addition and quaternary ammonium salts thereof are prepared, for example, (a) when R is a hydrogen atom and X 1 is a C 1-4 alkyl group, by treatment of a 3-thianaphthenyl-alkylamine of the general formula with an aldehyde or ketone of the general formula X 1 COX 2 in the presence of p-toluenesulphonic acid and toluene, followed by treatment with an acid; (b) when R and X 1 are hydrogen atoms, by reduction of a 3,4-dihydrothianaphtheno[2,3-c]pyridine or 3,4-dihydro- 5H - benzothieno[2,3 - c] - azepine derivative of the general formula and (c) when R is a C 1-4 alkyl or C 7-11 aralkyl group, by treatment of a compound of the first general formula above wherein R is a hydrogen atom with a compound of the general formula RX in which R is a C 1-4 alkyl or C 7-11 aralkyl group and X is a halogen atom, followed optionally by conversion of the product to a pharmaceutically acceptable acid addition or quaternary ammonium salt thereof. Pharmaceutical compositions having antipsychotic, anti - hypertensive and central nervous system stimulant activity comprise, as active ingredient, a 1,2,3,4-tetrahydrobenzothieno[2,3-c]pyridine or 1,2,3,4-tetrahydro-5H- benzothieno[2,3-c]azepine derivative of the first general formula above or a pharmaceutically acceptable acid addition or quaternary ammonium salt thereof, and a pharmaceutically acceptable carrier. 1 - Methyl - 3,4 - dihydrothianaphtheno[2,3-c]- pyridine is prepared by reduction of 3-cyanomethylthianaphthene with lithium aluminium hydride, treatment of the resulting #-(3-thianaphthenyl) - ethylamine with acetic anhydride and treatment of the N-[13-(3-thianaphtenyl)- ethyl]acetamide so obtained with phosphorus oxychloride and phosphorus pentoxide.
机译:1,210,106。 1,2,3,4-四氢苯并噻吩并[2,3-c]吡啶和1,2,3,4-四氢-5H-苯并i [2,3-c] c庚因衍生物。 COLGATEPALMOLIVE CO.1968年3月6日[1967年3月8日(2); 1968年2月6日(2)],第10892/68号。标题C2C。通式为A和A 1的新型1,2,3,4-四氢苯并噻吩并[2,3-c]吡啶和1,2,3,4-四氢-5H-苯并噻吩并[2,3-c]]相同或不同,且为氢或卤素原子或羟基,硝基,C 1-4烷基,C 1-3烷氧基或三氟甲基; m为1或2; R为氢原子或C 1-4烷基,C 7-11芳烷基,-(CH 2)n OH(其中n为2至6),B-Am,-COOR 1,-COBAm或a基,其中B为单化学键或C 1-6亚烷基。 R 1为C 1-4烷基,二-(C 1-4烷基)氨基-C 1-4烷基,羟基-C 1-4烷基,C 3-6烯基,C 7-11芳烷基,C 3- 7个环烷基或C 3-7环烷基-C 1-4烷基;并且Am是(a)-NR 2 R 3,其中R 2和R 3相同或不同并且为氢原子或C 1-4烷基,二-(C 1-4烷基)-氨基-C 1-4烷基,羟基-C 1-4烷基,C 3-6烯基,C 3-7环烷基或C 3-7环烷基-C 1-4烷基; (b)吗啉代,吡咯烷基,哌啶子基,N-C 1-4烷基-哌嗪子基,N-(苯基-C 1-4烷基)。哌嗪子基或N-(羟基C 1-4烷基)-哌嗪子基团; (c)通过核碳原子与B键合的哌啶基或吡咯烷基。 X 1和X 2相同或不同,且为氢原子或C 1-4烷基,苯基,卤代或烷氧基取代的苯基,C 7-11芳烷基,哌啶基,吡啶基,呋喃基,吡咯,吡咯烷基或B- Am基团,条件是当X 1和R 2均为氢原子时,X 2不是氢原子;及其药学上可接受的酸加成盐和季铵盐,例如,(a)当R为氢原子且X 1为C 1-4烷基时,通过通式3-噻吩并噻吩基-烷基胺的处理而制备。在对甲苯磺酸和甲苯的存在下用通式X 1 COX 2的醛或酮,然后用酸处理; (b)当R和X 1为氢原子时,通过还原3,4-二氢噻吩并[2,3-c]吡啶或3,4-二氢-5H-苯并噻吩并[2,3-c]-的氮杂环庚烷衍生物在通式(c)中,当R为C 1-4烷基或C 7-11芳烷基时,通过用通式RX的化合物处理上述第一通式的化合物(其中R为氢原子),其中R是C 1-4烷基或C 7-11芳烷基,X是卤原子,然后任选地将产物转化成可药用的酸加成盐或它们的季铵盐。具有抗精神病药,抗高血压药和中枢神经系统刺激活性的药物组合物包含作为活性成分的1,2,3,4-四氢苯并噻吩并[2,3-c]吡啶或1,2,3,4-四氢-5H -以上第一通式的苯并噻吩并[2,3-c] a庚因衍生物或其药学上可接受的酸加成盐或季铵盐,以及药学上可接受的载体。 1-甲基-3,4-二氢噻吩并[2,3-c]-吡啶是通过用氢化铝锂还原3-氰基甲基噻吩并用乙酸酐处理所得的#-(3-噻吩基)-乙胺并用乙酸酐处理而制得的。用三氯氧化磷和五氧化二磷得到的N- [13-(3-噻吩基)-乙基]乙酰胺。

著录项

  • 公开/公告号GB1210106A

    专利类型

  • 公开/公告日1970-10-28

    原文格式PDF

  • 申请/专利权人 COLGATE-PALMOLIVE COMPANY;

    申请/专利号GB19680010892

  • 发明设计人

    申请日1968-03-06

  • 分类号C07D333/58;C07D495/04;

  • 国家 GB

  • 入库时间 2022-08-23 10:29:24

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