RU2003137596A - Карбаматы 2-гетероциклил-1,2-этандиолов - Google Patents

Карбаматы 2-гетероциклил-1,2-этандиолов Download PDF

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RU2003137596A
RU2003137596A RU2003137596/04A RU2003137596A RU2003137596A RU 2003137596 A RU2003137596 A RU 2003137596A RU 2003137596/04 A RU2003137596/04 A RU 2003137596/04A RU 2003137596 A RU2003137596 A RU 2003137596A RU 2003137596 A RU2003137596 A RU 2003137596A
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oxocarboxamide
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Йонг-Моон ЧОЙ (US)
Йонг-Моон ЧОЙ
Ки-Хо ЛИ (KR)
Ки-Хо ЛИ
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    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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Claims (17)

1. Карбаматы 2-гетероциклил-1,2-этандиолов формулы
Figure 00000001
где А обозначает гетероциклический фрагмент, необязательно замещенный одним или более заместителей, выбираемых из группы, состоящей из алкила, арила, галогена, тригалогенметила, тригалогенметокси, триалкилсилила, S(O)R, SO2R, SO2NRR’, SO3R, SR, NO2, NRR’, OR, CN, C(O)R, OC(O)R, NHC(O)R, CO2R и CONRR’, где R и R’, независимо, обозначают водород, алкил или арил;
B1 и В2, независимо, обозначают гидрокси или OCONR1R2, при условии, что B1 и В2 не одновременно обозначают гидрокси, и R1 и R2, независимо, выбирают из группы, состоящей из водорода, гидрокси, алкила, алкокси, алкиларила, арилалкила, арила и арилокси и их энантиомеров, их энантиомерные смеси,
и их фармацевтически приемлемые соли.
2. Соединение по п.1, отличающееся тем, что указанное соединение представляет собой чистый энантиомер или энантиомерную смесь, в которой один энантиомер преобладает.
3. Соединение по п.1, отличающееся тем, что B1 и В2 обозначают OCONH2.
4. Соединение по п.1, отличающееся тем, что только один из B1 и В2 обозначает OCONH2.
5. Соединение по п.1, отличающееся тем, что А выбирают из группы, состоящей из
Figure 00000002
Figure 00000003
где каждый из R3, R4 и R5, независимо, выбирают из группы, состоящей из водорода, алкила и арила, а Х выбирают из серы, кислорода и азота.
6. Соединение по п.5, отличающееся тем, что А обозначает
Figure 00000004
где каждый из R3, R4 и R5, независимо, выбирают из группы, состоящей из водорода, алкила и арила, а Х выбирают из серы, кислорода и азота.
7. Соединение по п.6, отличающееся тем, что А обозначает
Figure 00000005
где каждый из R3, R4 и R5, независимо, выбирают из группы, состоящей из водорода, алкила и арила.
8. Соединение по п.1, которое представляет собой (±)-(2-(5-хлор-2-тиенил)-2-карбамоилоксиэтил)оксокарбоксамид.
9. Соединение по п.1, которое представляет собой (+)-(2R)-(2-(5-хлор-2-тиенил)-2-карбамоилоксиэтил)оксокарбоксамид.
10. Соединение по п.1, которое представляет собой (-)-(2S)-(2-(5-хлор-2-тиенил)-2-карбамоилоксиэтил)оксокарбоксамид.
11. Соединение по п.1, которое представляет собой (2-(5-трифторметил-2-тиенил)-2-карбамоилоксиэтил)оксокарбоксамид.
12. Соединение по п.1, которое представляет собой (2-(5-бром-2-тиенил)-2-карбамоилоксиэтил)оксокарбоксамид.
13. Фармацевтическая композиция для лечения расстройств центральной нервной системы, содержащая эффективное количество соединения по п.1.
14. Фармацевтическая композиция по п.13, отличающаяся тем, что подлежащее лечению расстройство центральной нервной системы выбирают из группы, состоящей из судорог, эпилепсии, удара, нейрогенных болей и мышечного спазма.
15. Фармацевтическая композиция по п.13, отличающаяся тем, что указанное соединение представляет собой чистый энантиомер или энантиомерную смесь, в которой преобладает один энантиомер.
16. Способ лечения расстройства центральной нервной системы, который заключается во введении больному, нуждающемуся в таком лечении, эффективного количества соединения по п.1.
17. Способ по п.16, отличающийся тем, что указанное соединение представляет собой чистый энантиомер или энантиомерную смесь, в которой преобладает один энантиомер.
RU2003137596/04A 2001-06-25 2002-06-18 Карбаматы 2-гетероциклил-1,2-этандиолов RU2298552C2 (ru)

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US7598279B2 (en) * 2005-04-22 2009-10-06 Sk Holdings Co., Ltd. Neurotherapeutic azole compounds
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US6841569B2 (en) 2005-01-11
KR100912521B1 (ko) 2009-08-18
CA2451151C (en) 2011-08-09
ATE373475T1 (de) 2007-10-15
DE60222552D1 (de) 2007-10-31
CA2451151A1 (en) 2003-01-03
US20050065193A1 (en) 2005-03-24
RU2298552C2 (ru) 2007-05-10
JP4378616B2 (ja) 2009-12-09
BR0210678A (pt) 2004-09-21
WO2003000247A1 (en) 2003-01-03
CN1536992A (zh) 2004-10-13
EP1406605A1 (en) 2004-04-14
ES2294140T3 (es) 2008-04-01
JP2005502609A (ja) 2005-01-27
EP1406605B1 (en) 2007-09-19
US20030078235A1 (en) 2003-04-24
EP1406605A4 (en) 2005-10-26
MXPA04000008A (es) 2004-05-21
KR20040018271A (ko) 2004-03-02
CN100338055C (zh) 2007-09-19
DE60222552T2 (de) 2008-06-26

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