SU422137A3 - Способ получения 1- - Google Patents

Способ получения 1-

Info

Publication number: SU422137A3
Authority: SU; USSR - Soviet Union
Prior art keywords: acid; hydrochloride; methylphenoxy; chloroform; solution
Prior art date: 1969-10-06

Application number

SU1705731A

Other languages

English (en)

Russian (ru)

Original Assignee

Иностранцы Герберт Кеппе, Карл Цейле , Альбрехт Энгельхард

Иностранна фирма К.Х. Берингер Зон

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1969-10-06

Filing date

1970-10-05

Publication date

1974-03-30

1970-10-05 Application filed by Иностранцы Герберт Кеппе, Карл Цейле , Альбрехт Энгельхард, Иностранна фирма К.Х. Берингер Зон filed Critical Иностранцы Герберт Кеппе, Карл Цейле , Альбрехт Энгельхард

1974-03-30 Application granted granted Critical

1974-03-30 Publication of SU422137A3 publication Critical patent/SU422137A3/ru

Links

238000000034 method Methods 0.000 title description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
239000000243 solution Substances 0.000 description 10
229910001868 water Inorganic materials 0.000 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
150000001875 compounds Chemical class 0.000 description 8
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
-1 2-cyano-5-methylphenoxy Chemical group 0.000 description 5
238000001816 cooling Methods 0.000 description 4
ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 4
125000004093 cyano group Chemical group *C#N 0.000 description 4
229910052943 magnesium sulfate Inorganic materials 0.000 description 4
235000019341 magnesium sulphate Nutrition 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000012074 organic phase Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000002253 acid Substances 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
239000012954 diazonium Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
235000010288 sodium nitrite Nutrition 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
150000001989 diazonium salts Chemical class 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
230000001766 physiological effect Effects 0.000 description 2
NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 2
SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
239000011975 tartaric acid Substances 0.000 description 2
LNSCNEJNLACZPA-UHFFFAOYSA-N 2,3-dihydroxy-2,3-bis(2-methylphenyl)butanedioic acid Chemical compound CC1=CC=CC=C1C(O)(C(O)=O)C(O)(C(O)=O)C1=CC=CC=C1C LNSCNEJNLACZPA-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
VXIDBKBIIFWZHF-UHFFFAOYSA-N CC(C)(C)NCC(COC(C=C(C)C=C1)=C1N)O.Cl.Cl Chemical compound CC(C)(C)NCC(COC(C=C(C)C=C1)=C1N)O.Cl.Cl VXIDBKBIIFWZHF-UHFFFAOYSA-N 0.000 description 1
KHAHNSYDGLCSBO-UHFFFAOYSA-N CC(C)NCC(COC(C=C(C)C=C1)=C1N)O.Cl.Cl Chemical compound CC(C)NCC(COC(C=C(C)C=C1)=C1N)O.Cl.Cl KHAHNSYDGLCSBO-UHFFFAOYSA-N 0.000 description 1
OBHJEQFRDSQQSN-UHFFFAOYSA-N CCC(C)(C)NCC(COC(C=C(C)C=C1)=C1N)O.Cl.Cl Chemical compound CCC(C)(C)NCC(COC(C=C(C)C=C1)=C1N)O.Cl.Cl OBHJEQFRDSQQSN-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
241001331845 Equus asinus x caballus Species 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
229910000365 copper sulfate Inorganic materials 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical group N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 1
239000012071 phase Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical class CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
238000000746 purification Methods 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
235000011044 succinic acid Nutrition 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- A61K31/275—Nitriles; Isonitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/53—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and hydroxy groups bound to the carbon skeleton
- E—FIXED CONSTRUCTIONS
- E05—LOCKS; KEYS; WINDOW OR DOOR FITTINGS; SAFES
- E05D—HINGES OR SUSPENSION DEVICES FOR DOORS, WINDOWS OR WINGS
- E05D15/00—Suspension arrangements for wings
- E05D15/40—Suspension arrangements for wings supported on arms movable in vertical planes
- E05D15/44—Suspension arrangements for wings supported on arms movable in vertical planes with pivoted arms and vertically-sliding guides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Animal Behavior & Ethology (AREA)
Mechanical Engineering (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

SU1705731A 1969-10-06 1970-10-05 Способ получения 1- SU422137A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19691950351 DE1950351C3 (de)	1969-10-06	1969-10-06	l-(2-Cyano-5-methylphenoxy)-2-hydroxy-3-aIkylaminopropane, Verfahren zu ihrer Herstellung sowie diese enthaltende Arzneimittel

Publications (1)

Publication Number	Publication Date
SU422137A3 true SU422137A3 (ru)	1974-03-30

Family

ID=5747463

Family Applications (6)

Application Number	Title	Priority Date	Filing Date
SU1705731A SU422137A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1699774A SU426360A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1705732A SU423291A3 (2)	1969-10-06	1970-10-05
SU1705733A SU421182A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1705730A SU417938A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1699773A SU503507A3 (ru)	1969-10-06	1971-09-21	Способ получени 1-(2-циано-5-метилфенокси)-2-окси-3-алкиламинопропанов

Family Applications After (5)

Application Number	Title	Priority Date	Filing Date
SU1699774A SU426360A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1705732A SU423291A3 (2)	1969-10-06	1970-10-05
SU1705733A SU421182A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1705730A SU417938A3 (ru)	1969-10-06	1970-10-05	Способ получения 1-
SU1699773A SU503507A3 (ru)	1969-10-06	1971-09-21	Способ получени 1-(2-циано-5-метилфенокси)-2-окси-3-алкиламинопропанов

Country Status (13)

Country	Link
JP (1)	JPS501262B1 (2)
AT (10)	AT308072B (2)
BG (8)	BG17528A3 (2)
CH (1)	CH542814A (2)
CS (1)	CS162731B2 (2)
DE (1)	DE1950351C3 (2)
DK (1)	DK128237B (2)
ES (9)	ES384244A1 (2)
PL (3)	PL84642B1 (2)
RO (9)	RO59186A (2)
SE (1)	SE375094B (2)
SU (6)	SU422137A3 (2)
YU (1)	YU34516B (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2660811C1 (ru) *	2017-03-21	2018-07-10	Общество с ограниченной ответственностью Научно-производственное предприятие "Резонанс" (ООО НПП "Резонанс")	Индукторная электрическая машина

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FI101950B1 (fi)	1996-12-12	1998-09-30	Uponor Bv	Menetelmä ja laitteisto kierrätettävän muovimateriaalin hyödyntämiseksi ja puristinlaitteella tehty muovituote

1969
- 1969-10-02 BG BG018263A patent/BG17528A3/xx unknown
- 1969-10-06 DE DE19691950351 patent/DE1950351C3/de not_active Expired
1970
- 1970-09-23 CS CS646770A patent/CS162731B2/cs unknown
- 1970-10-02 BG BG018262A patent/BG17294A3/xx unknown
- 1970-10-02 BG BG018264A patent/BG17295A3/xx unknown
- 1970-10-02 BG BG018265A patent/BG17296A3/xx unknown
- 1970-10-02 CH CH1461770A patent/CH542814A/de not_active IP Right Cessation
- 1970-10-02 BG BG018261A patent/BG17527A3/xx unknown
- 1970-10-02 BG BG018266A patent/BG17529A3/xx unknown
- 1970-10-02 BG BG015776A patent/BG17293A3/xx unknown
- 1970-10-02 BG BG018268A patent/BG17531A3/xx unknown
- 1970-10-03 ES ES384244A patent/ES384244A1/es not_active Expired
- 1970-10-05 SE SE1347570A patent/SE375094B/xx unknown
- 1970-10-05 DK DK505570A patent/DK128237B/da not_active IP Right Cessation
- 1970-10-05 JP JP8675670A patent/JPS501262B1/ja active Pending
- 1970-10-05 SU SU1705731A patent/SU422137A3/ru active
- 1970-10-05 PL PL17334270A patent/PL84642B1/pl unknown
- 1970-10-05 SU SU1699774A patent/SU426360A3/ru active
- 1970-10-05 PL PL14378570A patent/PL84252B1/pl unknown
- 1970-10-05 YU YU244470A patent/YU34516B/xx unknown
- 1970-10-05 SU SU1705732A patent/SU423291A3/ru active
- 1970-10-05 PL PL17334370A patent/PL84637B1/pl unknown
- 1970-10-05 SU SU1705733A patent/SU421182A3/ru active
- 1970-10-05 SU SU1705730A patent/SU417938A3/ru active
- 1970-10-06 AT AT1052371A patent/AT308072B/de not_active IP Right Cessation
- 1970-10-06 AT AT1052571A patent/AT306695B/de not_active IP Right Cessation
- 1970-10-06 RO RO6727170A patent/RO59186A/ro unknown
- 1970-10-06 RO RO6727270A patent/RO58534A/ro unknown
- 1970-10-06 AT AT1053071A patent/AT306700B/de not_active IP Right Cessation
- 1970-10-06 AT AT900970A patent/AT302274B/de not_active IP Right Cessation
- 1970-10-06 RO RO6726870A patent/RO58532A/ro unknown
- 1970-10-06 AT AT1052871A patent/AT306698B/de not_active IP Right Cessation
- 1970-10-06 AT AT1052671A patent/AT306696B/de not_active IP Right Cessation
- 1970-10-06 AT AT1053171A patent/AT306701B/de not_active IP Right Cessation
- 1970-10-06 AT AT1052771A patent/AT306697B/de not_active IP Right Cessation
- 1970-10-06 RO RO6461670A patent/RO56983A/ro unknown
- 1970-10-06 RO RO6726970A patent/RO59185A/ro unknown
- 1970-10-06 RO RO6728970A patent/RO58550A/ro unknown
- 1970-10-06 RO RO6727070A patent/RO58533A/ro unknown
- 1970-10-06 AT AT1052971A patent/AT306699B/de not_active IP Right Cessation
- 1970-10-06 RO RO6727370A patent/RO58548A/ro unknown
- 1970-10-06 AT AT1052471A patent/AT306694B/de not_active IP Right Cessation
- 1970-10-06 RO RO6727470A patent/RO58549A/ro unknown
1971
- 1971-05-13 ES ES391137A patent/ES391137A1/es not_active Expired
- 1971-05-13 ES ES391141A patent/ES391141A1/es not_active Expired
- 1971-05-13 ES ES391138A patent/ES391138A1/es not_active Expired
- 1971-05-13 ES ES391136A patent/ES391136A1/es not_active Expired
- 1971-05-13 ES ES391135A patent/ES391135A1/es not_active Expired
- 1971-05-13 ES ES391139A patent/ES391139A1/es not_active Expired
- 1971-05-13 ES ES391134A patent/ES391134A1/es not_active Expired
- 1971-05-13 ES ES391140A patent/ES391140A1/es not_active Expired
- 1971-09-21 SU SU1699773A patent/SU503507A3/ru active

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2660811C1 (ru) *	2017-03-21	2018-07-10	Общество с ограниченной ответственностью Научно-производственное предприятие "Резонанс" (ООО НПП "Резонанс")	Индукторная электрическая машина

Also Published As

Publication number	Publication date
ES384244A1 (es)	1973-01-01
RO58550A (2)	1975-08-15
DK128237B (da)	1974-03-25
ES391134A1 (es)	1973-07-16
RO59185A (2)	1976-01-15
SU417938A3 (ru)	1974-02-28
BG17295A3 (bg)	1973-07-25
SU423291A3 (2)	1974-04-05
ES391135A1 (es)	1973-07-16
AT306696B (de)	1973-04-25
BG17528A3 (bg)	1973-11-10
SU421182A3 (ru)	1974-03-25
PL84637B1 (en)	1976-04-30
RO58548A (2)	1975-09-15
PL84642B1 (en)	1976-04-30
BG17531A3 (bg)	1973-11-10
AT306700B (de)	1973-04-25
SU400082A3 (2)	1973-10-03
RO59186A (2)	1976-01-15
JPS501262B1 (2)	1975-01-16
DE1950351C3 (de)	1978-12-21
YU34516B (en)	1979-09-10
AT306695B (de)	1973-04-25
RO58533A (2)	1975-08-15
CH542814A (de)	1973-10-15
ES391137A1 (es)	1973-07-16
DE1950351B2 (de)	1978-04-27
ES391136A1 (es)	1973-07-16
SU361563A3 (2)	1972-12-07
ES391138A1 (es)	1973-07-16
SE375094B (2)	1975-04-07
AT306699B (de)	1973-04-25
AT306697B (de)	1973-04-25
SU503507A3 (ru)	1976-02-15
ES391139A1 (es)	1973-07-16
RO58534A (2)	1975-09-15
AT306694B (de)	1973-04-25
SU400081A3 (2)	1973-10-03
BG17296A3 (bg)	1973-07-25
PL84252B1 (en)	1976-03-31
BG17529A3 (bg)	1973-11-10
ES391140A1 (es)	1973-07-16
RO58532A (2)	1975-09-15
DE1950351A1 (de)	1971-04-29
AT302274B (de)	1972-10-10
AT306701B (de)	1973-04-25
ES391141A1 (es)	1973-07-16
RO56983A (2)	1974-12-15
SU426360A3 (ru)	1974-04-30
CS162731B2 (2)	1975-07-15
BG17293A3 (bg)	1973-07-25
AT308072B (de)	1973-06-25
BG17294A3 (bg)	1973-07-25
RO58549A (2)	1975-08-15
BG17527A3 (bg)	1973-11-10
AT306698B (de)	1973-04-25
YU244470A (en)	1979-02-28

Publication	Publication Date	Title
UA66359C2 (uk)	2004-05-17	Спосіб одержання рацемічних або оптично активних сполук
Albertson et al.	1949	A synthesis of DL-proline
CA2295800A1 (en)	1999-01-21	Resolution of amines
CN1434800A (zh)	2003-08-06	吡啶－1－氧化物衍生物及其转化为药物活性化合物的方法
Elliott	1949	126. The stereochemistry of an oxazoline derivative of threonine. Improvement of a recent threonine synthesis
DE69010285T2 (de)	1994-10-13	Als Spasmolytica geeignete Dibenzothiazepin-Derivate.
SU606549A3 (ru)	1978-05-05	Способ получени фенилалкиламинов или их солей
JP4598276B2 (ja)	2010-12-15	ラセミ化方法
SU422137A3 (ru)	1974-03-30	Способ получения 1-
JPS595577B2 (ja)	1984-02-06	チカンサレテイルサンカンシキアミノアルコ−ルノセイホウ
NO124430B (2)	1972-04-17
CA1110653A (en)	1981-10-13	Optical resolution of amino acids into optical antipodes
SU440824A1 (2)	1974-08-25
US2574505A (en)	1951-11-13	Process of preparing 2, 2-diphenyl-3-methyl-4-dimethylamino butyronitrile
EP0612716A1 (fr)	1994-08-31	Procédé pour la préparation d'un aminoalcool optiquement pur
US2574150A (en)	1951-11-06	Acenaphthenyl amino alcohols
JPS63290873A (ja)	1988-11-28	４−アミノ−６−フルオロクロマン−４−カルボン酸エステルおよびその誘導体
US2671798A (en)	1954-03-09	2, 2-diphenyl-3-methyl-4-chlorobutyronitrile and processes for preparing the same
US2428239A (en)	1947-09-30	Alkamine derivatives of meta aminomethyl benzoic acid
US4029786A (en)	1977-06-14	Morpholine derivatives for treating depression
US2876261A (en)	1959-03-03	Alpha-di-chloroacetamido-beta-chloro-p-nitropropiophenone and method of production
DE69500758T2 (de)	1998-02-26	Substituierte bizyklische Oxazol- und Thiazol-Äther
US2030373A (en)	1936-02-11	Derivatives of thiazole and process of preparing the same
JP2767295B2 (ja)	1998-06-18	インドール―３―カルボニトリル化合物の製造方法
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