RU2009106934A - Производное аминофосфата и модулятор рецептора s1p, содержащий его в качестве активного ингредиента - Google Patents
Производное аминофосфата и модулятор рецептора s1p, содержащий его в качестве активного ингредиента Download PDFInfo
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- RU2009106934A RU2009106934A RU2009106934/04A RU2009106934A RU2009106934A RU 2009106934 A RU2009106934 A RU 2009106934A RU 2009106934/04 A RU2009106934/04 A RU 2009106934/04A RU 2009106934 A RU2009106934 A RU 2009106934A RU 2009106934 A RU2009106934 A RU 2009106934A
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- Prior art keywords
- chloro
- phenyl
- amino
- general formula
- monoester
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- 239000004480 active ingredient Substances 0.000 title claims 3
- 229940075993 receptor modulator Drugs 0.000 title claims 2
- 150000003839 salts Chemical class 0.000 claims abstract 10
- 150000001875 compounds Chemical class 0.000 claims abstract 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 6
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract 6
- 239000000126 substance Substances 0.000 claims abstract 6
- MVFMRYKTUMERBI-GOSISDBHSA-N [(2r)-2-amino-5-[2-chloro-4-[3-(trifluoromethyl)phenyl]sulfanylphenyl]-2-methylpentyl]phosphonic acid Chemical compound C1=C(Cl)C(CCC[C@](N)(C)CP(O)(O)=O)=CC=C1SC1=CC=CC(C(F)(F)F)=C1 MVFMRYKTUMERBI-GOSISDBHSA-N 0.000 claims abstract 4
- 125000005843 halogen group Chemical group 0.000 claims abstract 4
- 229910052731 fluorine Inorganic materials 0.000 claims abstract 3
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract 3
- 229910052736 halogen Inorganic materials 0.000 claims abstract 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 3
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 3
- 125000004434 sulfur atom Chemical group 0.000 claims abstract 3
- ZASRRQNLUNFIEQ-QGZVFWFLSA-N [(2r)-2-amino-4-[2-chloro-4-[3-(trifluoromethyl)phenoxy]phenyl]-2-methylbutyl]phosphonic acid Chemical compound C1=C(Cl)C(CC[C@](N)(C)CP(O)(O)=O)=CC=C1OC1=CC=CC(C(F)(F)F)=C1 ZASRRQNLUNFIEQ-QGZVFWFLSA-N 0.000 claims abstract 2
- FKZMFPPSMMVXRY-QGZVFWFLSA-N [(2r)-2-amino-4-[2-chloro-4-[3-(trifluoromethyl)phenyl]sulfanylphenyl]-2-methylbutyl]phosphonic acid Chemical compound C1=C(Cl)C(CC[C@](N)(C)CP(O)(O)=O)=CC=C1SC1=CC=CC(C(F)(F)F)=C1 FKZMFPPSMMVXRY-QGZVFWFLSA-N 0.000 claims abstract 2
- QUBWWLOWROPKST-HXUWFJFHSA-N [(2r)-2-amino-5-[2-chloro-4-(3-ethylphenyl)sulfanylphenyl]-2-methylpentyl]phosphonic acid Chemical compound CCC1=CC=CC(SC=2C=C(Cl)C(CCC[C@@](C)(N)CP(O)(O)=O)=CC=2)=C1 QUBWWLOWROPKST-HXUWFJFHSA-N 0.000 claims abstract 2
- POGSNGDJNSPATF-GOSISDBHSA-N [(2r)-2-amino-5-[2-chloro-4-[3-(trifluoromethyl)phenoxy]phenyl]-2-methylpentyl]phosphonic acid Chemical compound C1=C(Cl)C(CCC[C@](N)(C)CP(O)(O)=O)=CC=C1OC1=CC=CC(C(F)(F)F)=C1 POGSNGDJNSPATF-GOSISDBHSA-N 0.000 claims abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims 1
- 102000011011 Sphingosine 1-phosphate receptors Human genes 0.000 claims 1
- 108050001083 Sphingosine 1-phosphate receptors Proteins 0.000 claims 1
- PSXRHAAZPJORMC-HXUWFJFHSA-N [(2r)-2-amino-5-[2-chloro-4-[3-(trifluoromethyl)phenyl]sulfanylphenyl]-2-propylpentyl]phosphonic acid Chemical compound C1=C(Cl)C(CCC[C@](N)(CCC)CP(O)(O)=O)=CC=C1SC1=CC=CC(C(F)(F)F)=C1 PSXRHAAZPJORMC-HXUWFJFHSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000008177 pharmaceutical agent Substances 0.000 claims 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
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Abstract
1. Аминофосфатное производное, представленное общей формулой (1) ! [химическая формула 1] ! ! в которой R1 представляет собой атом хлора или неразветвленную алкильную группу, содержащую 1-3 атомов углерода, необязательно замещенных галогеном; R2 представляет собой атом фтора или атом хлора; R3 представляет собой неразветвленную алкильную группу, содержащую 1-3 атомов углерода; Х представляет собой атом кислорода или атом серы, а n обозначает 2 или 3, или его фармацевтически приемлемая соль или гидрат. ! 2. Аминофосфатное производное по п.1, отличающееся тем, что соединение представленное общей формулой (1), имеет общую формулу (1а): ! [химическая формула 2] !! в которой R3, Х и n имеют приведенные выше значения, или его фармацевтически приемлемая соли, или гидрат. ! 3. Аминофосфатное производное по п.1 или 2, отличающееся тем, что в общей формуле (1) или (1a) R3 представляет собой метильную группу, или его фармацевтически приемлемая соль, или гидрат. ! 4. Аминофосфатное производное по п.1, отличающееся тем, что указанное соединение, представленное общей формулой (1), представляет собой: ! 1) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенокси)фенил]-2-метилпентилфосфоновой кислоты, ! 2) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-метилпентилфосфоновой кислоты, ! 3) моноэфир (R)-2-амино-4-[2-хлор-4-(3-трифторметилфенокси)фенил]-2-метилбутилфосфоновой кислоты, ! 4) моноэфир (R)-2-амино-4-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-метилбутилфосфоновой кислоты, ! 5) моноэфир (R)-2-амино-5-[2-хлор-4-(3-этилфенилтио)фенил]-2-метилпентилфосфоновой кислоты, ! 6) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-метилпентилфосфоновой кислоты или ! 7) мон�
Claims (7)
1. Аминофосфатное производное, представленное общей формулой (1)
[химическая формула 1]
в которой R1 представляет собой атом хлора или неразветвленную алкильную группу, содержащую 1-3 атомов углерода, необязательно замещенных галогеном; R2 представляет собой атом фтора или атом хлора; R3 представляет собой неразветвленную алкильную группу, содержащую 1-3 атомов углерода; Х представляет собой атом кислорода или атом серы, а n обозначает 2 или 3, или его фармацевтически приемлемая соль или гидрат.
3. Аминофосфатное производное по п.1 или 2, отличающееся тем, что в общей формуле (1) или (1a) R3 представляет собой метильную группу, или его фармацевтически приемлемая соль, или гидрат.
4. Аминофосфатное производное по п.1, отличающееся тем, что указанное соединение, представленное общей формулой (1), представляет собой:
1) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенокси)фенил]-2-метилпентилфосфоновой кислоты,
2) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-метилпентилфосфоновой кислоты,
3) моноэфир (R)-2-амино-4-[2-хлор-4-(3-трифторметилфенокси)фенил]-2-метилбутилфосфоновой кислоты,
4) моноэфир (R)-2-амино-4-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-метилбутилфосфоновой кислоты,
5) моноэфир (R)-2-амино-5-[2-хлор-4-(3-этилфенилтио)фенил]-2-метилпентилфосфоновой кислоты,
6) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-метилпентилфосфоновой кислоты или
7) моноэфир (R)-2-амино-5-[2-хлор-4-(3-трифторметилфенилтио)фенил]-2-пропилпентилфосфоновой кислоты; или их фармацевтически приемлемую соль, или гидрат.
5. Аминофосфатное производное по п.1, синтезированное с помощью стадии, допускающей взаимодействие соединения, представленного общей формулой (2)
[химическая формула 3]
в которой R1 представляет собой атом хлора или неразветвленную алкильную группу с 1-3 атомами углерода, необязательно замещенными галогенами, R2 представляет собой атом фтора или атом хлора, А представляет собой атом галогена, Х представляет собой атом кислорода или атом серы, а n означает 2 или 3
с соединением, представленным общей формулой (12)
[химическая формула 4]
в присутствии основания, стадию разложения полученного в результате продукта под действием кислот, защиту атома азота трет-бутоксикарбонильной группой с последующим восстановлением полученного продукта, стадию взаимодействия восстановленного продукта с соединением, представленным общей формулой (10)
в которой R6 представляет собой алкильную группу с 1-6 атомами углерода или бензильную группу, а также стадию, на которой полученный на предыдущей стадии продукт подвергают ацидолизу или обработке галоидсиланом;
или его фармацевтически приемлемая соль или гидрат.
6. Модулятор рецептора S1P, содержащий в качестве активного ингредиента аминофосфатное производное, или его фармацевтически приемлемую соль, или гидрат по любому из пп.1-5.
7. Фармацевтическое средство, содержащее в качестве активного ингредиента аминофосфатное производное, или его фармацевтически приемлемую соль, или гидрат по любому из пп.1-5.
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US7877152B2 (en) * | 2006-07-31 | 2011-01-25 | JusJas LLC | Bipolar stimulation/recording device with widely spaced electrodes |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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RU2566296C2 (ru) * | 2010-12-21 | 2015-10-20 | Керин Фармасьютикал Ко., Лтд. | Производное дифенилсульфида и фармацевтический продукт, который содержит его в качестве активного ингредиента |
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