SU389096A1 - - Google Patents
Info
- Publication number
- SU389096A1 SU389096A1 SU1680473A SU1680473A SU389096A1 SU 389096 A1 SU389096 A1 SU 389096A1 SU 1680473 A SU1680473 A SU 1680473A SU 1680473 A SU1680473 A SU 1680473A SU 389096 A1 SU389096 A1 SU 389096A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- alkyl
- aqueous
- hydrochloric acid
- calculated
- found
- Prior art date
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000002329 infrared spectrum Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 125000003106 haloaryl group Chemical group 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZNQYIJSZNTVZTF-UHFFFAOYSA-N 3-methyl-4-phenyl-1h-imidazol-2-one Chemical compound N1C(=O)N(C)C(C=2C=CC=CC=2)=C1 ZNQYIJSZNTVZTF-UHFFFAOYSA-N 0.000 description 1
- 108010091987 aposome Proteins 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- -1 phenylcarbamoylphenyl-amino-ketone Chemical compound 0.000 description 1
- GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1680473A SU389096A1 (enrdf_load_stackoverflow) | 1971-07-01 | 1971-07-01 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1680473A SU389096A1 (enrdf_load_stackoverflow) | 1971-07-01 | 1971-07-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU389096A1 true SU389096A1 (enrdf_load_stackoverflow) | 1973-07-05 |
Family
ID=20482650
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1680473A SU389096A1 (enrdf_load_stackoverflow) | 1971-07-01 | 1971-07-01 |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU389096A1 (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6337342B1 (en) | 1997-12-23 | 2002-01-08 | Astrazeneca Ab | Bis-aryl or heteroaryl indoles |
| US6346625B1 (en) | 1999-06-23 | 2002-02-12 | Astrazeneca Ab | Protein kinase inhibitors |
| US6458792B1 (en) | 1998-03-13 | 2002-10-01 | Astrazeneca Ab | Compounds |
| US6492406B1 (en) | 1999-05-21 | 2002-12-10 | Astrazeneca Ab | Pharmaceutically active compounds |
-
1971
- 1971-07-01 SU SU1680473A patent/SU389096A1/ru active
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6337342B1 (en) | 1997-12-23 | 2002-01-08 | Astrazeneca Ab | Bis-aryl or heteroaryl indoles |
| US6458792B1 (en) | 1998-03-13 | 2002-10-01 | Astrazeneca Ab | Compounds |
| US6492406B1 (en) | 1999-05-21 | 2002-12-10 | Astrazeneca Ab | Pharmaceutically active compounds |
| US6346625B1 (en) | 1999-06-23 | 2002-02-12 | Astrazeneca Ab | Protein kinase inhibitors |
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