RU99120174A - HYDROMETHYL DERIVATIVES 2-AMINO-1,2,3,4-TETRAGIDRONAPTALINE AS A CARDIOVASCULAR AGENT - Google Patents
HYDROMETHYL DERIVATIVES 2-AMINO-1,2,3,4-TETRAGIDRONAPTALINE AS A CARDIOVASCULAR AGENTInfo
- Publication number
- RU99120174A RU99120174A RU99120174/04A RU99120174A RU99120174A RU 99120174 A RU99120174 A RU 99120174A RU 99120174/04 A RU99120174/04 A RU 99120174/04A RU 99120174 A RU99120174 A RU 99120174A RU 99120174 A RU99120174 A RU 99120174A
- Authority
- RU
- Russia
- Prior art keywords
- compound according
- asterisk
- single bond
- alkyl group
- carbon atom
- Prior art date
Links
- 239000002327 cardiovascular agent Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims 4
- -1 NHCHO Chemical group 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000004432 carbon atoms Chemical group C* 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 claims 1
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 claims 1
- 208000008787 Cardiovascular Disease Diseases 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 0 CCCN(C(CC1)Cc2c1c(*)c(*)cc2)C(*)=O Chemical compound CCCN(C(CC1)Cc2c1c(*)c(*)cc2)C(*)=O 0.000 description 1
Claims (6)
где r является целым числом, выбранным из 5, 6 и 7
s является целым числом, выбранным из 2 и 3;
А представляет О или одинарную связь;
R'4, R'5 и R'6, одновременно или порознь, представляют водород, ОН, галоид, нитро, C1-C4 алкил, C1-C4 алкокси, C1-C4 алкилтио, NH2, моно- или ди-C1-C4 алкиламино, SH, C1-C4 алкилсульфонил, C1-C4 алкоксикарбонил, NHCHO, C1-C4 алкилкарбониламино, NHCONH2, C1-C4 алкилсульфониламино, C1-C4 алкиламиносульфонил, SO2NH2, NHSO2NH2, СООН, SO3H, CONH2, СН2ОН или фенил; или
R'4 и R'5, в орто положении друг к другу, образуют вместе цепь из 3 или 4 групп, выбранных из CT'T", СО, S, О и NT"', где T' представляет атом водорода или C1-C4 алкильную группу, Т" представляет атом водорода, C1-C4 алкильную группу или аминогруппу и Т"' представляет атом водорода или C1-C4 алкильную группу; или Т' вместе с соседними Т" или Т"' образует одинарную связь, или Т" вместе с соседними Т' или Т"' образует одинарную связь;
звездочкой отмечается асимметрический атом углерода;
и его фармацевтически приемлемые соли.1. The compound of the formula
where r is an integer selected from 5, 6 and 7
s is an integer selected from 2 and 3;
A represents O or a single bond;
R ′ 4 , R ′ 5 and R ′ 6 , either simultaneously or separately, represent hydrogen, OH, halo, nitro, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio, NH 2 , mono - or di C 1 -C 4 alkylamino, SH, C 1 -C 4 alkylsulfonyl, C 1 -C 4 alkoxycarbonyl, NHCHO, C 1 -C 4 alkylcarbonylamino, NHCONH 2 , C 1 -C 4 alkylsulfonylamino, C 1 -C 4 alkylaminosulfonyl, SO 2 NH 2 , NHSO 2 NH 2 , COOH, SO 3 H, CONH 2 , CH 2 OH, or phenyl; or
R ' 4 and R' 5 , in the ortho position to each other, together form a chain of 3 or 4 groups selected from CT'T ", CO, S, O and NT"', where T' represents a hydrogen atom or C 1 A C 4 alkyl group, T "represents a hydrogen atom, a C 1 -C 4 alkyl group or an amino group, and T" represents a hydrogen atom or a C 1 -C 4 alkyl group; either T 'together with the neighboring T' or T '' forms a single bond, or T 'together with the neighboring T' or T '' forms a single bond;
an asymmetric carbon atom is marked with an asterisk;
and its pharmaceutically acceptable salts.
где PG, r, s, A, R'4, R'5 и R'6 являются такими: как они определены по п. 1.4. The method of preparation of the compound according to claim 1, comprising removing the protection and the subsequent restoration of the compounds of formula
where PG, r, s, A, R ' 4 , R' 5 and R ' 6 are as follows: as defined in claim 1.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITMI97A0000415 | 1997-02-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
RU99120174A true RU99120174A (en) | 2001-06-27 |
Family
ID=
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