SU268299A1 - - Google Patents
Info
- Publication number
- SU268299A1 SU268299A1 SU1261745A SU1261745A SU268299A1 SU 268299 A1 SU268299 A1 SU 268299A1 SU 1261745 A SU1261745 A SU 1261745A SU 1261745 A SU1261745 A SU 1261745A SU 268299 A1 SU268299 A1 SU 268299A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- substituted
- aryl
- alkyum
- acyl
- alkyloxy
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 8
- -1 lower alkoxycarboyl Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 230000010933 acylation Effects 0.000 claims description 2
- 238000005917 acylation reaction Methods 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 239000012458 free base Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 238000002955 isolation Methods 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 2
- 230000026731 phosphorylation Effects 0.000 claims description 2
- 238000006366 phosphorylation reaction Methods 0.000 claims description 2
- 150000003223 pyridoxals Chemical class 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 239000013078 crystal Substances 0.000 description 12
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridine hydrochloride Substances [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 5
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- WLNBMPZUVDTASE-HXIISURNSA-N (2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanal;sulfuric acid Chemical compound [O-]S([O-])(=O)=O.O=C[C@H]([NH3+])[C@@H](O)[C@H](O)[C@H](O)CO.O=C[C@H]([NH3+])[C@@H](O)[C@H](O)[C@H](O)CO WLNBMPZUVDTASE-HXIISURNSA-N 0.000 description 1
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU268299A1 true SU268299A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU1213983A3 (ru) | Способ получени @ -ациламино-3-монозамещенных пропеноатов | |
| JPS6178778A (ja) | ４，５‐ジヒドロ‐４‐オキソ‐２‐〔（２‐ｔｒａｎｓ‐フエニルシクロプロピル）アミノ〕‐３‐フランカルボン酸とその誘導体 | |
| SU268299A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| JPH07116126B2 (ja) | ２，３‐ジアミノアクリロニトリル誘導体 | |
| RU2768824C1 (ru) | 2-(фенил(фенилимино)метил)изоиндолин-1,3-дион и способ его получения | |
| US4183943A (en) | Organic compounds | |
| SU608470A3 (ru) | Способ получени производных циклопропанола | |
| NO309479B1 (no) | Fremgangsmåte for fremstilling av (1S-(1R*,2S*,3R*))-N-(4- morfolinylsulfonyl)-L-fenylalanyl-3-(2-amino-4-tiazolyl)-N-((1- cykloheksylmetyl)-2,3-dihydroksy-5-metylheksyl)-L-alaninamid | |
| US2763652A (en) | Piperazinediones and methods for their preparation | |
| RU2571417C2 (ru) | Способ получения n-замещенной 2-амино-4-(гидроксиметилфосфинил)-2-бутеновой кислоты | |
| BG99161A (bg) | Метод и междинен продукт за пречистване на окситетрациклин | |
| EA011409B1 (ru) | Способ получения морфологически чистой модификации "н" натеглинида | |
| CN116162039B (zh) | 一种可见光介导的丁二酰胺类化合物的合成方法 | |
| US4017533A (en) | Diaminomaleonitrile derivatives and processes for preparing the same | |
| RU2777444C1 (ru) | 1-(Фенил(фенилимино)метил) пирролидин-2,5-дион и способ его получения | |
| SU1414849A1 (ru) | 5Н-5-Оксоимидазо(2,1-в)-1,3-бензотиазины и способ их получени | |
| RU2084441C1 (ru) | Способ получения кислотно-аддитивных солей труднорастворимых карбоновых кислот и аминов или аминокислот | |
| US4070478A (en) | Benzimidazole substituted alanines | |
| JPH07267950A (ja) | ５−クロロ−ｎ−（４，５−ジヒドロ−１ｈ−イミダゾール−２−イル）−２，１，３−ベンゾチアジアゾール−４−アミン又はその酸付加塩の製造方法 | |
| SU1432983A1 (ru) | Способ получени ариламидов N @ -защищенного аргинина | |
| SU252954A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| SU282173A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| SU274107A1 (ru) | Способ получения амидов сульфоланилкарбоновых кислот | |
| KR820002295B1 (ko) | N-(2-피롤리디닐 알킬) 치환벤즈아미드류의 제법 | |
| SU1490115A1 (ru) | Способ получени гидрохлорида N-ацетил-2-хлор-3-иминоиндолина |