Pyrimidotriazines
    1.
    发明授权
    Pyrimidotriazines 失效
    PYRIMIDOTRIAZINES

    公开(公告)号:US3813393A

    公开(公告)日:1974-05-28

    申请号:US26587972

    申请日:1972-06-23

    申请人: HOFFMANN LA ROCHE

    发明人: ANDREWS K TONG B

    IPC分类号: C07D487/04 C07D57/34

    CPC分类号: C07D487/04 Y10S514/869

    摘要: A NEW CLASS OF PYRIMIDOTRIAZINES IS DESCRIBED HAVING A GENERAL ANTI-INFLAMMARTORY ACTIVITY AND SPECIFIC COMPOUNDS THEREIN ALSO EXHIBIT A DIURETIC ACTIVITY. METHODS FOR THE PREPARATION OF THE INSTANT PYRIMIDOTRIAZINES ARE ALSO DESCRIBED. THE NEW PYRIMIDORTRIAZINES ARE OF THE FOLLOWING FORMULA

    WHEREIN R IS A TRIFLUOROMETHYL. LOWER ALKYL, ARYL OR LOWER ARALKYL GROUP, R1 IS A HYDROGEN ATOM OR A LOWER ALKYL, ARYL OR LOWER ARALKYL GROUP, R2 IS A HYDROGEN ATOM AND R3 IS A HYDROGEN ATOM OR A LOWER ALKYL, LOWER ALKENYL, LOWER ALKYLNYL, LOWER CYCLOALKYL, ARYL, LOWER ARALKYL, HYDROXYL, HYDROXY-(LOWER ALKYL) OR ACYL GROUP OR R2 AND R3 EACH REPRESENT A LOWER ALKYL GROUP WHICH MAY BE JOINED DIRECTLY OR THROUGH AN OXYGEN, NITROGEN OR SULFUR ATOM TO FORM WITH THE NITROGEN ATOM TO WHICH THEY ARE ATTACHED TO A 5MEMBERED OR 6-MEMBERED HETEROMONOCYCLIC RING.

    3-R1,5-(R2-N(-R3)-),7-R-PYRIMIDO(5,4-E)-AS-TRIAZINE

    Triazolo triazinones
    2.
    发明授权
    Triazolo triazinones 失效
    TRIAZOLO TRIAZINONES

    公开(公告)号:US3759910A

    公开(公告)日:1973-09-18

    申请号:US3759910D

    申请日:1970-12-09

    申请人: BAYER AG

    发明人: DICKORE K EUE L

    CPC分类号: C07D253/075 C07D487/04

    摘要: NEW 1,2,3,7 - TETRAHYDRO-(1,2,4)TRIAZOLO(3,2-C)(1,2,4)TRIAZINONE-(7) COMPOUNDS OF THE FORMULA

    2-R2,2-R3,3-R4,6-R1,7-(O=)-1,2,3,7-TETRAHYDRO-(1,2,4)-

    TRIAZOLO(3,2-C)(1,2,4)TRIAZINE

    IN WHICH:

    R1 IS HYDROGEN, SUBSTITUTED OR UNSUBSTITUTED ALKYL, ALKENYL, CYCLOALKYL, ARALKYL OR ARYL; R2 AND R3 INDIVIDUALLY ARE HYDROGEN, SUBSTITUTED OR UNSUBSTITUTED ALKYL, ALKENYL, CYCLOALKYL, CYCLOALKENYL OR ARALKYL; AND R2 AND R3 TAKEN TOGETHER, ARE ALKYLENE OF FROM 4 TO 7 RING CARBON ATOMS WHICH MAY CARRY ONE OR MORE ALKYL GROUP SUBSTITUENTS, AND R4 IS HYDROGEN, ALKYL, ALKENYL, ARALKYL OR SUBSTITUTED OR UNSUBSTITUTED SRYL

    ARE PREPARED BY A NOVEL SYNTHESIS BY REACTING THE CORRESPONDING DIAMINO DIHYDRO TRIAZINONE COMPOUND WITH AN OXO COMPOUND OF THE FORMULA

    R2-CO-R3

    IN THE PRESENCE OF A LOWER ALKANOIC ACID. THE NOVEL COMPOUNDS ARE OUTSTANDINGLY EFFECTIVE AS HERBICIDES, E.G., AS SELECTIVE HERBICIDES.

    Imidazo(1 2-b)-as-triazines
    4.
    发明授权
    Imidazo(1 2-b)-as-triazines 失效
    IMIDAZO(1 2-B)-AS-TRIAZINES

    公开(公告)号:US3631040A

    公开(公告)日:1971-12-28

    申请号:US3631040D

    申请日:1969-02-07

    发明人: LOEV BERNARD

    IPC分类号: C07D487/04 C07D57/34

    CPC分类号: C07D487/04

    摘要: 1,5-DIHYDRO-2,6-DIPHENYLIMIDAZO(1,2-B) - AS - TRIAZINES ARE PREPARED EITHER BY REACTION OF A PHENYLGLYOXAL AND AMINOGUANIDINE TO GIVE AN AMINOPHENYLTRIAZINE, FURTHER REACTION WITH A PHENACYL BROMIDE, AND REDUCTION WITH BOROHYDRIDE; OR DIRECTLY BY REACTION OF PHENACYL BROMIDE, AMINOGUANIDINE, AND HYDROGEN BROMIDE; AND SUBSEQUENT RING-CLOSURE IN BASE. THE PRODUCTS AE ANTIDEPRSSANTS.

    7-Phenyl-3-{8 2-(dialkylamino)-alkyl{9 -3,4-dihydroas-triazino{8 4,3-a{9 {8 1,4{9 benzodiazepin-2(1h)-ones
    5.
    发明授权
    7-Phenyl-3-{8 2-(dialkylamino)-alkyl{9 -3,4-dihydroas-triazino{8 4,3-a{9 {8 1,4{9 benzodiazepin-2(1h)-ones 失效
    7-苯基-3- {8 2-(二烷基氨基) - 烷基{9,3,4-二氢 - 三氮杂嗪{8,43-a {9 {8 1,4 {9苯并二氮杂-2(1h) - 酮

    公开(公告)号:US3882112A

    公开(公告)日:1975-05-06

    申请号:US39864173

    申请日:1973-09-19

    申请人: UPJOHN CO

    IPC分类号: C07D487/04 C07D57/34

    CPC分类号: C07D487/04

    摘要: Compounds of the formula:

    WHEREIN N IS 1 OR 2; WHEREIN R is hydrogen, alkyl of one to three carbon atoms, inclusive, or together

    IS PYRROLIDINO, PIPERIDINO, METHYLPIPERAZINO, OR MORPHOLINO; WHEREIN R1 is hydrogen or alkyl as defined above; and wherein R2 and R3 are hydrogen, alkyl as defined above, fluorine, chlorine, bromine, nitro, trifluoromethyl, or alkylthio in which alkyl is defined as above, are prepared by reacting a compound of the formula:

    WHEREIN R1, R2, and R3 are defined as above, with sodium hydride and then with

    WHEREIN X is chlorine, bromine, or iodine, and n, R or

    ARE DEFINED AS ABOVE TO OBTAIN THE COMPOUND OF THE FORMULA ABOVE. The compounds of the formula 11 above and the pharmacologically acceptable acid addition salt thereof have sedative and tranquilizing activity.

    摘要翻译: 下式的化合物:

    Tricyclic benzodiazepines
    7.
    发明授权
    Tricyclic benzodiazepines 失效
    三氯苯甲酸

    公开(公告)号:US3818003A

    公开(公告)日:1974-06-18

    申请号:US21511872

    申请日:1972-01-03

    申请人: UPJOHN CO

    发明人: SZMUSZKOVICZ J

    CPC分类号: C07D487/04

    摘要: Novel 7-substituted-3,5-dihydro-as-triazino(4,3-a)(1,4)benzodiazepin-2(1H)-ones, 7-substituted-3,5-dihydro-astriazino(4,3-a)(1,4)benzodiazepine-2(1H) -thiones, the 6-oxide derivatives thereof, the intermediate 5-substituted-2,3-dihydro2-thioxo-1H-1,4-benzodiazepine-1-acetic acid alkyl esters, pharmacologically acceptable acid addition salts thereof, and processes for the production thereof. The compounds of this invention and the pharmacologically acceptable acid addition salts thereof are central nervous system depressants which are useful as sedatives, hypnotics, tranquilizers, muscle relaxants and anticonvulsants. They are also useful as feed additives for increasing growth rate and feed efficiency of livestock and poultry, milk production in mammals and egg production in birds.

    摘要翻译: 新的7-取代-3,5-二氢 - 三嗪并[4,3-a] - [1,4]苯并二氮杂-2(1H) - ,7-取代-3,5-二氢 - 4,3-a] [1,4]苯并二氮杂-2(1H) - 噻喃,其6-氧化物衍生物,中间体5-取代-2,3-二氢-2-硫代-1H-1,4-苯并二氮杂 -1-乙酸烷基酯,其药理学上可接受的酸加成盐及其制备方法。 本发明化合物及其药理学上可接受的酸加成盐是可用作镇静剂,安眠药,镇静剂,肌肉松弛剂和抗惊厥药的中枢神经系统抑制剂。 它们也可用作饲料添加剂,用于提高家畜和家禽的生长速度和饲料效率,哺乳动物产奶量和鸡蛋生产量。

    Benzimidazole derivatives as fungicidal active compounds
    8.
    发明授权
    Benzimidazole derivatives as fungicidal active compounds 失效
    苯并咪唑衍生物作为杀真菌活性化合物

    公开(公告)号:US3725406A

    公开(公告)日:1973-04-03

    申请号:US3725406D

    申请日:1971-10-12

    申请人: UNIV CALIFORNIA

    发明人: BOSE E WHITE E

    IPC分类号: C07D487/04 C07D57/34

    CPC分类号: C07D487/04

    摘要: The method of manufacture, method of use and fungicidal active compounds are described herein. The active compounds have the following formula:

    D R A W I N G
    WHEREIN R can be selected from the group consisting of hydrogen, sodium, potassium and ammonium.

    摘要翻译: 本文描述了制造方法,使用方法和杀真菌活性化合物。 活性化合物具有下式: