• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:

    公开号:SU778710A3
    申请号:SU782700462
    申请日:1978-12-25
    公开日:1980-11-07
    发明作者:Буржери Ги；Лакур Ален；Пурриа Бернар；Кристин Брежон Женевьев
    申请人:Делаланд С.А. (Фирма)；
    IPC主号:
    专利说明:

    Yield, 37%; m. 180 ° C.
    Found,%: C 53.41; H 5.31; N 4.75.
    CuHisClNOs.
    Calculated,%: C 53.59; H 5, N 4.46.
    b) Hydrated 5-acetam dichlorohydrate, ido-4,7-dimethoxin6- (4-methylstiperazinoethoxy) -benzofuran.
    During 8 hours, a solution of L5.5 g (0.06 mol) of 5-acetamido-6- (2-chloroethoxy) -4,7-dimethoxybenzofuran prepared in the previous example and 15 g (0.15%) is heated under reflux. mol) N-met.ilpiperaein in 100 ml of toluene. It is filtered, evaporated in vacuo, the residue is again placed in alcohol and hydrochloric alcohol is added. Filtered and crystallized in absolute alcohol.
    Yield 55%; m. 160 ° C
    Found,%: C 46.76; H 6.73; N 8.34;
    C.gHsgClaNsOs + 9/4 H, O.
    Calculated,%: C 46.48; H 6.88; N 8.56.
    c) 5-Ami-noch, 7-d. mimeto1Xi-6-1 2- (iN-methylP | IperazInil) -ethOxy-bbnzofura1n.
    A solution of 16.9 g of hydrated 5-acetamido, 7-dimethoxy-b- (4-methylpiperazinoetoic) benzofuran in 60 mm 2 N. of hydrochloric acid is heated under reflux for 4 hours. Alkalinize with concentrated alkali sodium, extracted with chloroform and evaporated the solvent. Get 9 g. Crystal and the call of a new product:
    The yield is 100%, so pl. 62 ° C, mol. v.337, 394.
    Found,%: C 60, i56; H 7.62; N 12.67; Calculated,%: iC 60.87; H 7.51; N 12.53.
    d) 4,7-Dimethoxy-5-amINO-M-methylcarba .moyl-6- 2- (S - methylpiperazinyl) - this is benzofuran.
     A mixture of 9 g of 5-th HO-4,7-dimethoy-6-: 2 - (: M-methylpipera 3 | ynyl) -ecoic benzofuran and 1.7 g of methyl isocyanate in 100 ml of toluene is heated to 70 ° C for 4 h . Then the solvent is added, the residue is introduced into isopropyl ether, filtered, crystallized in a mixture of 40-60% benzene and heptane.
    . 8 g of the desired product is obtained. Yield 80%; m.p. 1: 18 ° C; a pier at. 410.46. Found,%: C 55.48; H 7.08; N 13.93;
    C, 9 "2 N40s-f" 0.
    Calculated,%: C 55.59; H 7.37; N 13.65.
    Example 2. 4,7-Dimethoxn-5- (N-methylcarbamylamino) -b- (pineridinoethox) -benzofuran.
    a) Hydrochloride 5-acetamido-4,7-dimethoxn-6- (piperidi) noethoxy) -benzofuraia.
    A mixture of 25.1 g (0.1 mol) of 5-acetamido-4, 7-dimeto: Xin6-ethoxybenzofuran, 22.2 g (0.16 mol) of 2-1 piper1, or "ochloroethane and
    41, .6 g (0.3 mol) of potassium carbonate in 250 ml of acetone. It is then filtered, the solvent is evaporated, the residue is taken up again in acetone and 20 ml of hydrochloric ethanol 7N are added. Filtered
    and crystallized in 400 ml of propanol.
    Yield 33%, so pl. 260 ° C;
    Found,%: C 57.35; H 7.03; N 7.08;
    C, 9H27CIN205.
    Calculated,%: C 67.21; H 6.82; N 7.02.
    b) b-Amino-4,7-dimeTO dichlorohydrate (XI6- (2-piperid.inoethoxy) -beisofuran.
    Within 10 hours, a solution of 25.1 g (0.4 mol) of 5-acetamido-4,7-dimethoxy-6- (2-piperidinoethoic) -benzofur1n prepared in the previous step, in 200 ml of salt, is heated under reflux. Acid acid 2N. Then neutralized with concentrated soda, extracted with ethyl acetate.
    The solvent is evaporated, the residue is again placed in acetone and 30 ml of hydrochloric ethanol 7iN is added. Filter and crystallize in ethanol.
    Yield 43%, mp, 203 ° C.
    Found,%: C 51.72; H 6.63; N 6.81;
    Cl7H26Cl2N O4.
    Calculated,%: C 51.48; H i6,74; N 6.91. c) 4.7 - Dimethoxy-5-1M-methylcarbamide-6- (2-p.i.peridinoethoxy) -benzofuran.
    The mixture is incubated at 80-90 ° C for 3 hours at a mixture of I6 g (0.05 mol) in an autoclave.
    5-ami1No-4,7-dimethoxy-6- (2- and I1-peridino-etoxy) -benzofuran, prepared at the previous stage, and 3.2 ml (0.055 mol) of methyl isocyanate in 530 ml of toluene. Then, the solvent is evaporated, the resulting oil is crystallized in petroleum ether and recrystallized in 1-isopropyl ether, m.p. 120 ° C
    Yield 37%. Found,%: C 60.42; H 7.29; N 11.30;
    CigH27 N3O5.
    Calculated,%: C 60.46; H 7.21; N 11.13.
    OSSN /
    NH-CO-NC

    O-CH-lCH lmI
    OCHjR4:
    Table
    odH,
    0- o-sn2- (n,) (
    X
    axis.
    where m and have the above
    To
    values are reacted with a zocyanate of the formula
    RgNCO (III)
    where R2 is as defined above, in toluene at 70-90 ° C.
    The source of information taken into account in the examination:
    1. Weigand-Hilgetag. Experimental methods in organic chemistry, M., “Chemistry, 1968, p. 377.
    Priorities featured:
    12: 07.76 with the group -N o-dialkyl g 2
    the amino group, where aliyl contains 1 to 3 carbon atoms, or a heterocyclic radical, namely pyrrole. idyl, pyridium, or 4-mepilli: a perazine ring, t is an integer equal to 1 or 2, and Ra is methyl or ethyl;
    06.26.77 with group - hetero K2
    cyclic radical, namely hexamethyleneimine, heptamethyleneimine or 4-methylniperidine ring, t is an integer equal to 1 or 2, and R2 is methyl or ethyl.
    权利要求:
    Claims (1)
    [1]
    The formula of the invention derivatives of amino Method for producing alkoxybenzofuran of the General formula n nn-Oo-nC R 3 K1
    0- <1H 2 - (CH 2 ) t- ^ x * 2 (I) ιΰ dialkyl-amino group, where the alkyl contains 1-3 carbon atoms, or a heterocyclic radical, namely the pyrrolidine piperidine, hexamethyleneimine, heptamethyleneimine, 4-methylpiperidine or 4 methylpiperazitide R 2 is methyl or ethyl;
    t is an integer of 1 or 2;
    a new ring, characterized in that the compound of the formula
    Ί (and)
    RgNCO have the above meanings, are reacted with an isocyanate of the formula (III) where R 2 - has the above meanings, in toluene medium at a temperature of 70-90 ° C.
    Source of information taken into account during the examination:
    1. Weigand Hilgetag. Methods of experiment in organic chemistry, M., "Chemistry", 1968, p. 377.
    Priorities by attributes:
    5 12.07.76 when the group is a dialkylamino group, where the alkyl contains 1-3 carbon atoms, or a heterocyclic radical, namely a pyrrolidine, piperidine 10 or 4-methylpiper azine ring, t is an integer equal to 1 or 2, and R 3 - methyl or ethyl;
    06/27/77 when the group —— hetero K 2
    15 cyclic radical, namely hexamethyleneimine, heptamethyleneimine or 4-methylpiperidine ring, m is an integer equal to 1 or 2, and R 2 is methyl or ethyl.
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    同族专利:
    公开号 | 公开日
    SE8300445L|1983-01-28|
    US4113951A|1978-09-12|
    AU516331B2|1981-05-28|
    JPS6028831B2|1985-07-06|
    SE8300446L|1983-01-28|
    SU655312A3|1979-03-30|
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    DE2730593A1|1978-01-19|
    ES470783A1|1979-09-01|
    NL7707713A|1978-01-16|
    SU747425A3|1980-07-23|
    ES460600A1|1978-12-01|
    CH627175A5|1981-12-31|
    GR61634B|1978-12-04|
    SE441268B|1985-09-23|
    SE8300446D0|1983-01-28|
    ES470784A1|1979-01-16|
    SE8300445D0|1983-01-28|
    GB1545725A|1979-05-16|
    CA1100958A|1981-05-12|
    JPS5412365A|1979-01-30|
    SE7708041L|1978-01-13|
    CH625234A5|1981-09-15|
    LU77713A1|1978-01-31|
    AU2695477A|1979-01-18|
    IT1115363B|1986-02-03|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    BE786362A|1971-07-26|1973-01-17|Delalande Sa|NEW DERIVATIVES OF GAMMA-DIALKYLAMINOALKOXY-6 DIMETHOXY-4,7 BENZOFURANS, THEIR PREPARATION PROCESS AND THEIR APPLICATION IN THERAPEUTICS|FR2447378A1|1979-01-23|1980-08-22|Delalande Sa|Antihypertensive and vasodilating 4,7-di:methoxy benzofuran - prepd. from phenyl piperazine and epoxy or halo alkoxy benzofuran|
    DE3710469A1|1987-03-30|1988-10-20|Basf Ag|NEW BENZOFURANE DERIVATIVES AND THERAPEUTICAL AGENTS CONTAINING THEM|
    DE3716734A1|1987-05-19|1988-12-01|Basf Ag|OPTICAL RECORDING MEDIUM THAT HAS A REFLECTOR LAYER CONTAINING SILICON PHTHALOCYANINE DERIVATIVE|
    DE3724756A1|1987-07-25|1989-02-09|Basf Ag|BASICLY SUBSTITUTED BENZOFURANCARBONIC ACID AMIDES, PROCESS FOR THEIR PRODUCTION AND THERAPEUTIC AGENTS CONTAINING THE SAME|
    DE3727736A1|1987-08-20|1989-03-02|Basf Ag|NEW BENZOFURANE DERIVATIVES AND THERAPEUTICAL AGENTS CONTAINING THEM|
    AU2320400A|1999-02-08|2000-08-25|Shionogi & Co., Ltd.|Cyclic amine derivatives and uses thereof|
    US20030171413A1|2000-08-17|2003-09-11|Owen David Alan|Bicyclic heteroaromatic derivatives for the treatment of immune and inflammatory disorders|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR7621287A|FR2358143B1|1976-07-12|1976-07-12|
    FR7719658A|FR2396008B2|1977-06-27|1977-06-27|
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