• 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:
    SPRAY FOR WELFARE 2- (THIENIL2) - Ida 2- (taE1D-3) EPIPASONS of the general form w | - eM2-tH-NH2 where R is hydrogen or alkyl with 1-4 carbon atoms, by means of hydrogen and nitrovinyl-terfe. on the general formula I; H RNS -N02 where R has the indicated values, characterized in that, in order to simplify the process, the latter is carried out by catalytic hydrogenation in two stages, first at a temperature of 35 ° C and a pressure of 20 atm in the presence of palladium, platinum or rhodium, addition in the amount of 1:
    公开号:SU1148562A3
    申请号:SU823457191
    申请日:1982-06-25
    公开日:1985-03-30
    发明作者:Ан-Аршар Жиль；Эймес Ален；Валетт Жерар
    申请人:Санофи (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to an improved process for the preparation of 2- (thienyl-2) or 2- (thienyl-3) ethylamines, which are used as intermediates in the chemical and pharmaceutical industries.
    A known method for the preparation of 2- (thiens-1-2) ethylamine and its derivatives is carried out by treating 2- (thienyl) alkanol esters with phthalimide in the presence of a base and transamining 2- (phthalimicoethyl-2) thiophene or its derivatives by the action of amine lJ.
    Thus, treatment of 1- (thienyl2) -2-propanol tosylate with phthalimide in dimethylformamide in the presence of sodium carbonate at 80 ° C yields a phthalimide derivative in 44% yield, which is converted into 2- (thienyl-2) with thythylamine with yield 77%.,
    The disadvantage of this method is the low yield of the target product (34%).
    The closest to the invention to the technical essence is the method of obtaining 2- (thienyl-2) - or 2- (thienyl-3) ethyl Min of the formula
    TT-dHz-CH-NHz
    (I) r
    where R is hydrogen or alkyl with 1-4 carbon atoms,
    by reduction of 2- / 3-nitrovinylyl 3- / b-nitrovinyl-thiophene of the general formula

    CH -d-N02
    R
    where R - has the same values as lithium aluminum on the air. 40
    The disadvantages of this method are its high risk and the high cost of lithium aluminum hydride.
    The purpose of the invention is to simplify the process, which makes it possible to reduce the fire hazard of the process. I use less expensive reagents.
    This goal is achieved by the fact that, according to the method for producing 2- (thienyl-2) or 2- (thienyl-3) ethylamines 50 of the general formula t, catalytic hydrogenation Fei nitrovinylthiophene of the general formula P; in two steps — first, at a temperature and pressure of 20 atM, in the presence of palladium, barbine, or rhode, taken in an amount of 1: (100–10,000) relative to the substrate, in a mixture of acetic acid and ethanol, and the resulting oxime. general formula.
    -eH,
    HE
    (w)
    R
    where R has the indicated values, it is reduced at a temperature of 60 ° C and a pressure of 20 atm in the presence of Rene nickel in saturated methanol.
    P p and measures 1. Preparation of 2- (thienyl-2) ethylamine chlorrhydrate
    a / Oximes 2-thienyl-acetaldehyde, 100 g (0.645 mol) of 2- (thiens-1-2) nitroethylene in the form of a solution in 2 l of a mixture of acetic acid and ethanol (75/25) is hydrogenated in an autoclave at 35 C under a pressure of 20 bar the presence of 5 g of 5% palladium on coal until the end of absorption (about two hours). After filtering off the catalyst and washing with ethanol, the resulting solution is evaporated in vacuo at 50. The oily residue is dissolved in 500 ml of methylene chloride and the solution of the follower is passed through with aqueous 1 and. caustic soda solution, then water and finally evaporated, get 97 g of oximes (a mixture of syn + anti) (thienyl-2) acetaldehyde in the form of an orange-yellow oil, used without purification in the subsequent stage.,
    b / A mixture of oximes in a solution in 2 liters of methanol saturated with ammonia is hydrogenated in an autoclave at a pressure of 20 bar in the presence of 10 g of Rene nickel until the adsorption stops (about 20 hours). After filtering off the catalyst and washing it with methanol, the resulting solution is evaporated. The oily residue is dissolved in 500 mp of toluene. This organic phase is extracted with n. aqueous solution of hydrochloric acid. The aqueous acidic phase is alkalinized with 1N. an aqueous solution of caustic soda, then extracted with toluene. Adding to the combined organic phase a solution of gaseous hydrogen chloride in diisopropyl ether causes a precipitate to form, which is filtered, then dried. Thus, 68 g are obtained (yield 65% with respect to 2- (thienyl-2) -nitroethylene / 2- (thienyl) 3 hporohydrate; 3.; ethylamine in the form of white crystals. T.Sh1. 202 HP. C HgNSHCt 163.67. Calculated %: C 44.03; AND 6.15; N 8.55. Found,%: C 43.98; H 6.16; N 8.54. PRI mme R 2. Hydrochloride 2- (nie -3) ethylamine. Work under the conditions described in Example 1, but replacing the coal with Pd / LC or the 5% Pd / coal with hydrochloride at the compound with a Vyoso content of 66%. Mp. E HgNS-HCt 163.67.% Calculated: C 44.03; H 6.15; H 8.55. Found: C: 43.92; H 6.18;} 8.50. 24. Chlorohydrate G-methyl2- (thienyl-3) ethylamine. Work under the conditions described in measure 1, but replacing 5% Pt / on coal with 5% Pd /, get hydrous compound hydrate on coal with a yield of 81%. mp. C, H NS-HCI 177.69. Calculated,%: C 47.31; H 6.80; N 7.88. Found,%: C 47.55; H 6.85; N 7.92. -. -. The proposed method makes it possible to stop the process by eliminating flammable ether and explosive and expensive lithium aluminum hydride.
    权利要求:
    Claims (1)
    [1]
    METHOD FOR GETTING 2- (THienyl2) -or 2- (thienyl-3) ethylamines of general formula | where R is hydrogen or alkyl with 1-4 carbon atoms, by reduction of nitrovinylthiophe in the general formula I
    -4 * 4
    GT-CH-C-KOG * to where R has the indicated meanings, characterized in that, in order to simplify the process, the latter is carried out by catalytic hydrogenation in two stages, first at a temperature of 35 ° C and a pressure of 20 atm in the presence of palladium, platinum or rhodium taken in an amount of 1: (10010000) in relation to the substrate, in a mixture of acetic acid and ethanol, and then the resulting oxime of the general formula III rj-CHi-CN-OH
    TO.
    where R has the indicated meanings, is reduced at a temperature of 60 ° C and a pressure of 20 atm in the presence of Raney nickel in saturated ammonia methanol.
    . SU „1148562
    1 1148562
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    同族专利:
    公开号 | 公开日
    JPS5810575A|1983-01-21|
    EP0069002A1|1983-01-05|
    AU556916B2|1986-11-27|
    IL65984D0|1982-09-30|
    NO155345C|1987-03-18|
    CS236482B2|1985-05-15|
    PT75156B|1984-02-21|
    HU186867B|1985-10-28|
    KR840000539A|1984-02-25|
    FI822318L|1982-12-31|
    CA1205811A|1986-06-10|
    NZ200856A|1985-11-08|
    GR77203B|1984-09-11|
    PT75156A|1982-07-01|
    DE3266028D1|1985-10-10|
    ES8305348A1|1983-04-01|
    ES514220A0|1983-04-01|
    FR2508456A1|1982-12-31|
    DK153793B|1988-09-05|
    DK291782A|1982-12-31|
    IL65984A|1985-09-29|
    AU8475282A|1983-01-06|
    NO155345B|1986-12-08|
    FR2508456B1|1983-09-09|
    YU142982A|1984-12-31|
    FI822318A0|1982-06-29|
    ZA824618B|1983-04-27|
    DK153793C|1989-01-23|
    IE53278B1|1988-09-28|
    EP0069002B1|1985-09-04|
    AR231444A1|1984-11-30|
    IE821314L|1982-12-30|
    AT15369T|1985-09-15|
    JPH039914B2|1991-02-12|
    DD202711A5|1983-09-28|
    NO822228L|1983-01-03|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE2623174A1|1976-05-22|1977-12-01|Basf Ag|Primary amine prepn. from oximes - by hydrogenation in presence of ammonia with catalysts contg. aluminium and nickel and/or cobalt|NZ214698A|1984-12-31|1988-08-30|Merrell Dow Pharma|Thiophene derivatives and pharmaceutical compositions containing such|
    FR2608607B1|1986-12-23|1989-04-28|Sanofi Sa|PROCESS FOR THE PREPARATION OF THIENYLETHYLAMINES AND DITHIENYLETHYLAMINES THUS OBTAINED|
    NZ223583A|1987-02-26|1990-02-26|Merrell Dow Pharma|2- or 3-thienyl-or-furyl-2-propyn-1-amines and antihypertensive compositions|
    FR2622191B1|1987-10-22|1991-06-21|Sanofi Sa|PROCESS FOR THE PREPARATION OF N--2 ETHYLAMINE AND INTERMEDIATE PRODUCTS IN THIS PREPARATION|
    US4906756A|1988-05-10|1990-03-06|SyntexInc.|2-thiophene reduction and synthesis of thieno[3,2-c]pyridine derivatives|
    US5191090A|1990-01-25|1993-03-02|SyntexInc.|Preparation of 2-ethylamine derivatives and synthesis of thieno[3,2-c]pyridine derivatives therefrom|
    FR2664276B1|1990-07-04|1992-10-23|Sanofi Sa|GLYCIDIC THIENYL-2 DERIVATIVE, ITS PREPARATION METHOD AND ITS USE AS A SYNTHESIS INTERMEDIATE.|
    US5208252A|1992-07-24|1993-05-04|Ortho Pharmaceutical Corporation|Aminoethylthiophene derivatives|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR8113066A|FR2508456B1|1981-06-30|1981-06-30|
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