SU603331A3 - Способ получени рацемата -/2-бензгидрилэтил/ -/1-фенилэтил/-амина,его оптическиактивных антиподов или их солей - Google Patents
Способ получени рацемата -/2-бензгидрилэтил/ -/1-фенилэтил/-амина,его оптическиактивных антиподов или их солейInfo
- Publication number
- SU603331A3 SU603331A3 SU752174852A SU2174852A SU603331A3 SU 603331 A3 SU603331 A3 SU 603331A3 SU 752174852 A SU752174852 A SU 752174852A SU 2174852 A SU2174852 A SU 2174852A SU 603331 A3 SU603331 A3 SU 603331A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- optically active
- diphenylpropyl
- phenylethyl
- salts
- racemate
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 6
- 150000003839 salts Chemical class 0.000 title claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- -1 3,3-diphenylpropyl alcohol Chemical compound 0.000 claims description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- SLHSRCBFPHCSGL-UHFFFAOYSA-N (3-bromo-1-phenylpropyl)benzene Chemical compound C=1C=CC=CC=1C(CCBr)C1=CC=CC=C1 SLHSRCBFPHCSGL-UHFFFAOYSA-N 0.000 claims 1
- NENUCJVGUPDXPC-UHFFFAOYSA-N 3,3-diphenylpropyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCCC(C=1C=CC=CC=1)C1=CC=CC=C1 NENUCJVGUPDXPC-UHFFFAOYSA-N 0.000 claims 1
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000012429 reaction media Substances 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LUPKSZKBBIBTAR-UHFFFAOYSA-N 2,3-diphenylpropyl 4-methylbenzenesulfonate Chemical compound Cc1ccc(cc1)S(=O)(=O)OCC(Cc1ccccc1)c1ccccc1 LUPKSZKBBIBTAR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/27—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring having amino groups linked to the six-membered aromatic ring by saturated carbon chains
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Emergency Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HUCI1510A HU169507B (cs) | 1974-09-25 | 1974-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU603331A3 true SU603331A3 (ru) | 1978-04-15 |
Family
ID=10994536
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU752174852A SU603331A3 (ru) | 1974-09-25 | 1975-09-25 | Способ получени рацемата -/2-бензгидрилэтил/ -/1-фенилэтил/-амина,его оптическиактивных антиподов или их солей |
SU762386655A SU837319A3 (ru) | 1974-09-25 | 1976-08-03 | Способ получени оптических изомеров -(2-бЕНзгидРилэТил)- -(1-фЕНилэТил)-АМиНА или иХ СОлЕй |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU762386655A SU837319A3 (ru) | 1974-09-25 | 1976-08-03 | Способ получени оптических изомеров -(2-бЕНзгидРилэТил)- -(1-фЕНилэТил)-АМиНА или иХ СОлЕй |
Country Status (22)
Country | Link |
---|---|
JP (1) | JPS5159843A (cs) |
AR (2) | AR210586A1 (cs) |
AT (1) | AT337675B (cs) |
AU (1) | AU497358B2 (cs) |
BE (1) | BE833824A (cs) |
CH (2) | CH609323A5 (cs) |
CS (2) | CS186749B2 (cs) |
DD (1) | DD124874A5 (cs) |
DE (1) | DE2541184C2 (cs) |
DK (1) | DK429075A (cs) |
FI (1) | FI752595A (cs) |
FR (1) | FR2285865A1 (cs) |
GB (1) | GB1464209A (cs) |
HU (1) | HU169507B (cs) |
IL (1) | IL48120A (cs) |
IN (1) | IN141186B (cs) |
NL (1) | NL7511183A (cs) |
NO (1) | NO753246L (cs) |
PL (2) | PL107557B1 (cs) |
SE (1) | SE7510611L (cs) |
SU (2) | SU603331A3 (cs) |
YU (2) | YU37112B (cs) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2739376C1 (ru) * | 2020-07-24 | 2020-12-23 | Федеральное государственное бюджетное учреждение науки Институт элементоорганических соединений им. А.Н. Несмеянова Российской академии наук (ИНЭОС РАН) | Способ получения фендилина |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2862103D1 (en) * | 1977-08-19 | 1982-11-18 | Sandoz Ag | Propenyl amines, processes for their production and pharmaceutical compositions containing them |
FR2504524A1 (fr) * | 1981-04-22 | 1982-10-29 | Spofa Vereinigte Pharma Werke | N-(1-phenylethyl)-n-(3,3-diphenylpropyl)-hydroxylamines et procede pour leur preparation |
US6011068A (en) * | 1991-08-23 | 2000-01-04 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
US6313146B1 (en) | 1991-08-23 | 2001-11-06 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
US6001884A (en) * | 1991-08-23 | 1999-12-14 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
US5858684A (en) * | 1991-08-23 | 1999-01-12 | The Brigham And Women's Hospital, Inc. | Method of screening calcium receptor-active molecules |
US6031003A (en) * | 1991-08-23 | 2000-02-29 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
US5763569A (en) * | 1991-08-23 | 1998-06-09 | The Brigham And Women's Hospital, Inc | Calcium receptor-active molecules |
US5962314A (en) * | 1993-02-23 | 1999-10-05 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
DK1203761T3 (da) * | 1994-12-08 | 2005-04-11 | Nps Pharma Inc | Calciumreceptoraktive forbindelser |
US6057346A (en) * | 1994-12-12 | 2000-05-02 | The United States Of America As Represented By The Department Of Health And Human Services | Inhibition of retroviral LTR promoters by calcium response modifiers |
JP4117506B2 (ja) | 1996-05-01 | 2008-07-16 | エヌピーエス ファーマシューティカルズ インコーポレイテッド | 無機イオン活性化合物 |
WO2014031755A1 (en) * | 2012-08-21 | 2014-02-27 | The Board Of Regents Of The University Of Texas System | Fendiline derivatives and methods of use thereof |
-
1974
- 1974-09-25 HU HUCI1510A patent/HU169507B/hu unknown
-
1975
- 1975-09-16 CS CS7700003090A patent/CS186749B2/cs unknown
- 1975-09-16 CS CS7500006278A patent/CS186718B2/cs unknown
- 1975-09-16 DE DE2541184A patent/DE2541184C2/de not_active Expired
- 1975-09-17 AT AT711175A patent/AT337675B/de active
- 1975-09-17 IL IL48120A patent/IL48120A/xx unknown
- 1975-09-17 FI FI752595A patent/FI752595A/fi not_active Application Discontinuation
- 1975-09-18 AU AU84956/75A patent/AU497358B2/en not_active Expired
- 1975-09-18 IN IN1788/CAL/1975A patent/IN141186B/en unknown
- 1975-09-22 SE SE7510611A patent/SE7510611L/xx not_active Application Discontinuation
- 1975-09-23 DD DD188496A patent/DD124874A5/xx unknown
- 1975-09-23 NL NL7511183A patent/NL7511183A/xx not_active Application Discontinuation
- 1975-09-23 JP JP50115476A patent/JPS5159843A/ja active Pending
- 1975-09-23 FR FR7529069A patent/FR2285865A1/fr active Granted
- 1975-09-24 AR AR260504A patent/AR210586A1/es active
- 1975-09-24 YU YU2394/75A patent/YU37112B/xx unknown
- 1975-09-24 PL PL1975183553A patent/PL107557B1/pl unknown
- 1975-09-24 NO NO753246A patent/NO753246L/no unknown
- 1975-09-24 GB GB3915075A patent/GB1464209A/en not_active Expired
- 1975-09-24 CH CH950277A patent/CH609323A5/xx not_active IP Right Cessation
- 1975-09-24 PL PL1975197355A patent/PL108111B1/pl unknown
- 1975-09-24 CH CH1237175A patent/CH596139A5/xx not_active IP Right Cessation
- 1975-09-24 DK DK429075A patent/DK429075A/da unknown
- 1975-09-25 BE BE160382A patent/BE833824A/xx not_active IP Right Cessation
- 1975-09-25 SU SU752174852A patent/SU603331A3/ru active
-
1976
- 1976-08-03 SU SU762386655A patent/SU837319A3/ru active
- 1976-11-26 AR AR265488A patent/AR211558A1/es active
-
1981
- 1981-11-04 YU YU2611/81A patent/YU37115B/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2739376C1 (ru) * | 2020-07-24 | 2020-12-23 | Федеральное государственное бюджетное учреждение науки Институт элементоорганических соединений им. А.Н. Несмеянова Российской академии наук (ИНЭОС РАН) | Способ получения фендилина |
Also Published As
Publication number | Publication date |
---|---|
NL7511183A (nl) | 1976-03-29 |
IL48120A0 (en) | 1975-11-25 |
ATA711175A (de) | 1976-11-15 |
FR2285865B1 (cs) | 1980-05-30 |
GB1464209A (en) | 1977-02-09 |
AT337675B (de) | 1977-07-11 |
BE833824A (fr) | 1976-01-16 |
PL107557B1 (pl) | 1980-02-29 |
CS186749B2 (en) | 1978-12-29 |
FI752595A (cs) | 1976-03-26 |
PL108111B1 (pl) | 1980-03-31 |
AU8495675A (en) | 1977-03-24 |
YU239475A (en) | 1983-04-27 |
SU837319A3 (ru) | 1981-06-07 |
CH596139A5 (cs) | 1978-02-28 |
AR211558A1 (es) | 1978-01-30 |
IL48120A (en) | 1979-05-31 |
AU497358B2 (en) | 1978-12-07 |
CH609323A5 (en) | 1979-02-28 |
DK429075A (da) | 1976-03-26 |
YU261181A (en) | 1983-04-27 |
CS186718B2 (en) | 1978-12-29 |
JPS5159843A (en) | 1976-05-25 |
HU169507B (cs) | 1976-12-28 |
YU37112B (en) | 1984-08-31 |
NO753246L (cs) | 1976-03-26 |
DE2541184A1 (de) | 1976-04-15 |
DE2541184C2 (de) | 1984-05-10 |
AR210586A1 (es) | 1977-08-31 |
FR2285865A1 (fr) | 1976-04-23 |
IN141186B (cs) | 1977-01-29 |
DD124874A5 (cs) | 1977-03-16 |
YU37115B (en) | 1984-08-31 |
SE7510611L (sv) | 1976-03-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SU603331A3 (ru) | Способ получени рацемата -/2-бензгидрилэтил/ -/1-фенилэтил/-амина,его оптическиактивных антиподов или их солей | |
US3848030A (en) | Optical isomers of binaphthyl-phosphoric acids | |
GB1296493A (cs) | ||
JP2009509958A (ja) | ナフチルアルキルアミンによるα−(フェノキシ)フェニル酢酸誘導体の分割 | |
SU559642A3 (ru) | Способ получени алканоламинов или их солей в виде рацематов или оптически - активных антиподов | |
SU638252A3 (ru) | Способ получени производных аминоэтанола или их солей | |
US4224457A (en) | Process for manufacturing optically active sulfur-containing carboxylic acid | |
CA1056388A (en) | Resolution of racemic pantolactone | |
US4275217A (en) | Process for the preparation of optically active α-amino acids and their derivatives | |
CA2363284C (fr) | Procede de synthese de derives n-(mercaptoacyl)-amino-acides a partir d'acides acryliques alpha-subtitues | |
SU535899A3 (ru) | Способ получени -(1-бисарилалкиламиноалкил)-аралкоксибензиловых спиртов или их солей, рацематов или оптически активных антиподов | |
Fleš et al. | The Correlation of Configurations of Chloroamphenicol and D-Serine | |
JPS6351135B2 (cs) | ||
US4045450A (en) | Optical resolution of DL-pantolactone | |
JP2004530717A (ja) | (r)−(−)−2−ヒドロキシ−2−(2−クロロフェニル)酢酸の分割方法 | |
FI101880B (fi) | Menetelmä R(-) 2-(3-bentsoyylifenyyli)propionihapon muuttamiseksi S(+) -isomeeriksi | |
US3796748A (en) | Dehydroabietylammonium d-(-)-2-chloroacetylamino-2-(p-hydroxyphenyl)-acetate | |
JP2830364B2 (ja) | 光学活性1―ベンジル―3―ヒドロキシピロリジンの製造方法 | |
BR0008586B1 (pt) | processo de preparação de aminoácidos quirais e processo de preparação dos compostos de fórmula (a). | |
KR100235375B1 (ko) | 2-아미노나프티리딘 유도체의 광학 이성질체 제조 방법 | |
US4411836A (en) | Racemization of an α-methyl-β-acylthiopropionic acid | |
JPS6013736A (ja) | (±)−2−クロロプロピオン酸の光学分割法 | |
JPS63145256A (ja) | 光学活性ホモフエニルアラニンの製造法及び中間体 | |
SU550977A3 (ru) | Способ получени 1-изопропиламино-3-/4-(2алкоксикарбониламиноэтокси)-фенокси/-пропанолов-2 или их солей, рацематов, или оптически активных антиподов | |
JPH01221345A (ja) | マンデル酸誘導体の光学分割方法 |