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公开(公告)号:US3714163A
公开(公告)日:1973-01-30
申请号:US3714163D
申请日:1970-08-20
Applicant: ROUSSEL UCLAF
Inventor: CLEMENCE F , LE MARTRET O
IPC: C07D473/08 , C07H19/16 , C07D57/48 , C07D57/52
CPC classification number: C07D473/08 , C07H19/16
Abstract: As a new compound Beta -(theophylline ethyl) monosulfite having the formula
AND SALTS THEREOF WITH INORGANIC AND ORGANIC BASES, THEIR PROCESS OF PREPARATION AND AS AN ANTIBACTERIAL AGENT, THE TETRACYCLINE SALT OF Beta -(THEOPHYLLINE ETHYL) MONOSULFITE.Abstract translation: 作为具有下式的新型化合物β-(茶碱乙基)亚硫酸氢盐,其无机和有机物基质,它们的制备方法和抗菌剂,β-(乙酸乙酯)单体的四氢化萘盐。
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公开(公告)号:US3853875A
公开(公告)日:1974-12-10
申请号:US26278572
申请日:1972-06-14
Applicant: ROUSSEL UCLAF
Inventor: CLEMENCE F , LE MARTRET O
IPC: A61K31/495 , A61P9/08 , A61P9/12 , A61P25/02 , A61P43/00 , C07D277/56 , C07D295/08 , C07D295/088 , C07D91/32
CPC classification number: C07D295/088 , A61K31/495 , C07D277/56 , C07D295/08 , Y10S514/929
Abstract: X1 and X2, identical or different, representing hydrogen, a chlorine, bromine or iodine atom, an alkyl radical containing from 1 to 6 carbon atoms, an alkyloxy radical containing from 1 to 6 carbon atoms or a tribalogenomethyl group, or R represents a heterocycle containing a maximum of 6 links and capable of bearing 1 or more heteroatoms, as well as the salts of these compounds with a mineral or organic acid, and the process of preparation. These compounds have an adrenolytic and peripheral vasodilatatory activity.
wherein n represents the whole numbers 0, 1, 2, 3, 4 or 5, n'' represents the whole numbers 1, 2, 3, 4 or 5, m represents the whole numbers 0, 1, 2, 3, 4 or 5 and R represents a substituted or unsubstituted phenyl radical of general formula:
New esters of 2-alkyl thiazole 5-carboxylic acid of formula I:Abstract translation: 式I的2-烷基噻唑5-羧酸的新酯:
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公开(公告)号:US3778504A
公开(公告)日:1973-12-11
申请号:US3778504D
申请日:1971-10-08
Applicant: ROUSSEL UCLAF
Inventor: CLEMENCE F , LE MARTRET O
IPC: C07D213/82 , C07D235/06 , C07D235/08 , C07D235/18 , C07D307/68 , C07D333/38 , A61K27/00
CPC classification number: C07D213/82 , C07D235/06 , C07D235/08 , C07D235/18 , C07D307/68 , C07D333/38
Abstract: BENZIMIDAZOLES OF THE FORMULA
1-(2-R-PHENYL),2-R1,5-X'',6-X-BENZIMIDAZOLE
WHEREIN X AND X'' MAY BE DIFFERENT AND ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, HALOGEN, ALKYL, ALKOXY, TRIHALOMETHYL AND NITRO, R IS SELECTED FROM THE GROUP CONSISTING OF -COOH-, -COOR'', AND
-CO-N(-A)-B
R'' IS SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC AND HYDROXYLATED RESIDUE OF A GLYCOL, A AND B ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND OPTIONALLY SUBSTITUTED ALIPHATIC AND R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, LOWER ALIPHATIC HYDROCARBON, UNSUBSTITUTED AND POLYSUBSTITUTED ARYL, ARYLALIPHATIC, A THIENYL, A B-PYRIDYL AND A FURYL WITH THE PROVISO THAT WHEN R1 IS PHENYL, X'' AND X ARE OTHER THAN HALOGEN, ALKOXY AND TRIFLUOROMETHYL WHICH COMPOUNDS POSSESS ANTI-INFLAMMATORY AND ANTIVIRAL ACTIVITY AND A NOVEL PROCESS FOR THEIR PREPARATION.-
公开(公告)号:US3817999A
公开(公告)日:1974-06-18
申请号:US18461971
申请日:1971-09-28
Applicant: ROUSSEL UCLAF
Inventor: CLEMENCE F , LE MARTRET O
IPC: C07D295/192 , C07D87/34
CPC classification number: C07D295/192
Abstract: An amide of 2-hydroxy-3-methoxy-5-allyl-benzoic acid of the formula
WHEREIN R is selected from the group consisting of hydrogen, alkyl of 1 to 7 carbon atoms and acyl of an organic carboxylic acid of 1 to 18 carbon atoms, R1 and R2 taken together with the nitrogen atom form a heterocyclic which may contain another heteroatom, which products possess outstanding choleretic properties far superior to dehydrocholic acid.
D R A W I N GAbstract translation: 式WHEREIN R的2-羟基-3-甲氧基-5-烯丙基 - 苯甲酸的酰胺选自氢,1至7个碳原子的烷基和1至18个碳的有机羧酸的酰基 原子,R 1和R 2与氮原子一起形成可以含有另一个杂原子的杂环,该产物具有优于脱氢胆酸的优异的胆固醇性质。
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公开(公告)号:US3808213A
公开(公告)日:1974-04-30
申请号:US19356071
申请日:1971-10-28
Applicant: ROUSSEL UCLAF
Inventor: CLEMENCE F , LE MARTRET O
IPC: C07C57/72 , C07D211/56 , C07D295/185 , C07D51/70 , C07C103/22
CPC classification number: C07D295/185 , C07C57/72 , C07D211/56
Abstract: A COMPOUND SELECTED FROM THE GROUP CONSISTING OF ACETAMIDES OF THE FORMULA
CH*C-CH2-C(-C6H5)2-CO-N(-R)-CH(-R1)-CH2-N(-R2)-R3
WHEREIN R IS SELECTED FROM THE GROUP CONISTING OF HYDROGEN AND ALKYL OF 1 TO 4 CARBON ATOMS, R1 IS HYDROGEN, R2 IS ALKYL OF 1 TO 4 CARBON ATOMS AND R3 IS SELECTED FROM THE GROUP CONSISTING OF ALKYL OF 1 TO 4 CARBON ATOMS, ARYL AND ARALKYL OR THE GROUP
-N
MAY FORM A 6-MEMBERED NITROGEN-CONTAINING HETEROCYCLIC OR THE GROUP
-CH
MAY FROM A 6-MEMBERED NITROGEN-CONTAINING HETEROCYCLIC OR THE GROUP
-N(-R2-R3-)
MAY FORM A 5- TO 6-MEMBERED, NITROGEN-CONTAINING HETEROCYCLIC OPTIONALLY CONTAINING ANOTHER HETERO-ATOM AND THEIR NON-TOXIC, PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS WHICH HAVE INTENSE ANALGESIC ACTIVITY AND ACT AS POTENTIALIZERS FOR NEURO-SEDATIVES AND THEIR PREPARATION AND INTERMEDIATES THEREOF.
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