RU99116252A - METHOD OF OBTAINING IMIDAZOL DERIVATIVES - Google Patents
METHOD OF OBTAINING IMIDAZOL DERIVATIVESInfo
- Publication number
- RU99116252A RU99116252A RU99116252/04A RU99116252A RU99116252A RU 99116252 A RU99116252 A RU 99116252A RU 99116252/04 A RU99116252/04 A RU 99116252/04A RU 99116252 A RU99116252 A RU 99116252A RU 99116252 A RU99116252 A RU 99116252A
- Authority
- RU
- Russia
- Prior art keywords
- optionally substituted
- aryl
- alkyl
- formula
- substituted aryl
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N Imidazole Chemical class C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 9
- 125000000547 substituted alkyl group Chemical group 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000000962 organic group Chemical group 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 3
- 125000002252 acyl group Chemical group 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000005110 aryl thio group Chemical group 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- SJRJJKPEHAURKC-UHFFFAOYSA-N n-methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 claims 2
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 2
- AHQRTNSRMYQNSW-UHFFFAOYSA-N (3,5-dichlorophenyl) thiohypochlorite Chemical compound ClSC1=CC(Cl)=CC(Cl)=C1 AHQRTNSRMYQNSW-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims 1
Claims (6)
где R1 представляет водород, необязательно замещенный алкил, необязательно замещенный алкенил, необязательно замещенный арил, необязательно замещенный арилтио, необязательно замещенный гетероарил, необязательно замещенный гетероарилалкил, необязательно замещенный аралкил, необязательно замещенный ацил, необязательно замещенный карбамоил, необязательно замещенный алкоксикарбонил, -CH= NOH, -CH=NNH2 или -А-Х, где А представляет -CH2OCH2- или -СН2О- и Х представляет необязательно замещенный арил или COR5, где R5 представляет необязательно замещенный алкил, необязательно замещенный алкокси, необязательно замещенный арил или необязательно замещенный амино;
R2 представляет органическую группу; R3 представляет водород или органическую группу; и R4 представляет необязательно замещенный арил, включающий взаимодействие соединения формулы (I)
где R1, R2 и R3 имеют вышеуказанные значения, с соединением формулы (II)
R4-S-Hal
где R4 имеет вышеуказанные значения, и Hal представляет галоген, в присутствии основания.1. The method of obtaining the compounds of formula (III)
wherein R 1 represents hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted aryl, optionally substituted arylthio, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, optionally substituted aralkyl, optionally substituted acyl, optionally substituted carbamoyl, optionally substituted alkoxycarbonyl, -CH = NOH , -CH = NNH 2, or -A-X wherein A represents -CH 2 OCH 2 - or -CH 2 O- and X is an optionally substituted aryl or COR 5, where R 5 is optionally substituted ny alkyl, optionally substituted alkoxy, optionally substituted aryl or optionally substituted amino;
R 2 represents an organic group; R 3 represents hydrogen or an organic group; and R 4 is an optionally substituted aryl, comprising reacting a compound of formula (I)
where R 1 , R 2 and R 3 have the above values, with the compound of the formula (II)
R 4 -S-Hal
where R 4 has the above values, and Hal represents a halogen, in the presence of a base.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8/347507 | 1996-12-26 | ||
JP34750796 | 1996-12-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU99116252A true RU99116252A (en) | 2001-07-20 |
RU2188821C2 RU2188821C2 (en) | 2002-09-10 |
Family
ID=18390700
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU99116252/04A RU2188821C2 (en) | 1996-12-26 | 1997-12-19 | Method of synthesis of imidazole derivatives |
Country Status (18)
Country | Link |
---|---|
US (1) | US6057448A (en) |
EP (1) | EP0949249B1 (en) |
JP (1) | JP3378017B2 (en) |
KR (1) | KR100399463B1 (en) |
CN (1) | CN1100763C (en) |
AT (1) | ATE299498T1 (en) |
AU (1) | AU720862B2 (en) |
BR (1) | BR9714436A (en) |
CA (1) | CA2274530C (en) |
DE (1) | DE69733716T2 (en) |
ES (1) | ES2245005T3 (en) |
HU (1) | HUP0002067A3 (en) |
NO (1) | NO993154L (en) |
PL (1) | PL334294A1 (en) |
RU (1) | RU2188821C2 (en) |
TR (1) | TR199901474T2 (en) |
TW (1) | TW418194B (en) |
WO (1) | WO1998029395A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI232214B (en) * | 1998-04-16 | 2005-05-11 | Shionogi & Co | Preparation of aryl sulfenyl halide |
WO2001012594A1 (en) * | 1999-08-12 | 2001-02-22 | Nippon Finechemical Co., Ltd. | Processes for the preparation of aromatic sulfenyl chlorides and so forth |
WO2005016912A1 (en) * | 2003-08-19 | 2005-02-24 | Pfizer Inc. | An efficient microbial preparation of capravirine metabolites m4 and m5 |
CN106188046B (en) * | 2016-07-07 | 2018-09-28 | 安徽理工大学 | A kind of synthetic method of 3- arylthios imidazo [1,5-a] N- heterocyclic compounds that iodine promotes |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2606720B2 (en) * | 1987-03-13 | 1997-05-07 | 石原産業株式会社 | Imidazole compounds and pesticides containing them |
EP0293742B1 (en) * | 1987-06-05 | 1992-07-22 | BASF Aktiengesellschaft | Process for the production of 4-nitro-5-imidazolylethers and -thioethers |
US5223525A (en) * | 1989-05-05 | 1993-06-29 | Rhone-Poulenc Ag Company | Pesticidal 1-arylimidazoles |
JPH0389343A (en) * | 1989-09-01 | 1991-04-15 | Konica Corp | Heat developable color photosensitive material |
TW235963B (en) * | 1992-01-16 | 1994-12-11 | Shionogi & Co | |
WO1996010019A1 (en) * | 1994-09-26 | 1996-04-04 | Shionogi & Co., Ltd. | Imidazole derivative |
-
1997
- 1997-12-19 KR KR10-1999-7005828A patent/KR100399463B1/en not_active IP Right Cessation
- 1997-12-19 ES ES97949167T patent/ES2245005T3/en not_active Expired - Lifetime
- 1997-12-19 PL PL97334294A patent/PL334294A1/en not_active IP Right Cessation
- 1997-12-19 EP EP97949167A patent/EP0949249B1/en not_active Expired - Lifetime
- 1997-12-19 HU HU0002067A patent/HUP0002067A3/en unknown
- 1997-12-19 RU RU99116252/04A patent/RU2188821C2/en not_active IP Right Cessation
- 1997-12-19 BR BR9714436A patent/BR9714436A/en not_active Application Discontinuation
- 1997-12-19 CA CA002274530A patent/CA2274530C/en not_active Expired - Fee Related
- 1997-12-19 TR TR1999/01474T patent/TR199901474T2/en unknown
- 1997-12-19 AU AU78904/98A patent/AU720862B2/en not_active Ceased
- 1997-12-19 US US09/319,700 patent/US6057448A/en not_active Expired - Fee Related
- 1997-12-19 WO PCT/JP1997/004708 patent/WO1998029395A1/en active IP Right Grant
- 1997-12-19 AT AT97949167T patent/ATE299498T1/en not_active IP Right Cessation
- 1997-12-19 DE DE69733716T patent/DE69733716T2/en not_active Expired - Fee Related
- 1997-12-19 JP JP52981598A patent/JP3378017B2/en not_active Expired - Fee Related
- 1997-12-19 CN CN97181054A patent/CN1100763C/en not_active Expired - Fee Related
- 1997-12-26 TW TW086119794A patent/TW418194B/en active
-
1999
- 1999-06-24 NO NO993154A patent/NO993154L/en not_active Application Discontinuation
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