CH376486A - Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden - Google Patents

Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden

Info

Publication number: CH376486A
Authority: CH; Switzerland
Prior art keywords: radical; alkyl; formula; allyl; preparation
Prior art date: 1960-01-27

Application number

CH76960A

Other languages

German (de)

English (en)

Inventor

Franz Dr Litvan

Willy Dr Stoll

Original Assignee

Geigy Ag J R

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.)

1960-01-27

Filing date

1960-01-27

Publication date

1964-04-15

1960-01-27 Application filed by Geigy Ag J R filed Critical Geigy Ag J R

1960-01-27 Priority to CH76960A priority Critical patent/CH376486A/de

1961-01-25 Priority to GB2902/61A priority patent/GB906235A/en

1961-01-26 Priority to ES0264364A priority patent/ES264364A2/es

1961-01-26 Priority to ES0264365A priority patent/ES264365A2/es

1961-01-26 Priority to ES0264363A priority patent/ES264363A1/es

1961-01-26 Priority to BE599535A priority patent/BE599535A/fr

1961-04-25 Priority to FR859853A priority patent/FR1093M/fr

1964-04-15 Publication of CH376486A publication Critical patent/CH376486A/de

Links

238000000034 method Methods 0.000 title claims description 6
238000002360 preparation method Methods 0.000 title claims description 5
150000001408 amides Chemical class 0.000 title claims description 4
-1 cycloalkyl radical Chemical class 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 9
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 3
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
150000003335 secondary amines Chemical class 0.000 claims description 2
125000005265 dialkylamine group Chemical group 0.000 claims 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
150000008064 anhydrides Chemical class 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
150000004820 halides Chemical class 0.000 description 3
KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-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
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
BMFVGAAISNGQNM-UHFFFAOYSA-N isopentylamine Chemical compound CC(C)CCN BMFVGAAISNGQNM-UHFFFAOYSA-N 0.000 description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
XHFGWHUWQXTGAT-UHFFFAOYSA-N n-methylpropan-2-amine Chemical compound CNC(C)C XHFGWHUWQXTGAT-UHFFFAOYSA-N 0.000 description 2
RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
UUZNZXBSSVTRMY-UHFFFAOYSA-N 2-(4-prop-1-enyl-2-propoxyphenoxy)acetic acid Chemical compound C(CC)OC1=C(OCC(=O)O)C=CC(=C1)C=CC UUZNZXBSSVTRMY-UHFFFAOYSA-N 0.000 description 1
NNWUEBIEOFQMSS-UHFFFAOYSA-N 2-Methylpiperidine Chemical compound CC1CCCCN1 NNWUEBIEOFQMSS-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
LDCWGVLBCJEQMT-UHFFFAOYSA-N 2-methyl-n-(2-methylprop-2-enyl)prop-2-en-1-amine Chemical compound CC(=C)CNCC(C)=C LDCWGVLBCJEQMT-UHFFFAOYSA-N 0.000 description 1
NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 description 1
VXDHQYLFEYUMFY-UHFFFAOYSA-N 2-methylprop-2-en-1-amine Chemical compound CC(=C)CN VXDHQYLFEYUMFY-UHFFFAOYSA-N 0.000 description 1
PNPCRKVUWYDDST-UHFFFAOYSA-N 3-chloroaniline Chemical compound NC1=CC=CC(Cl)=C1 PNPCRKVUWYDDST-UHFFFAOYSA-N 0.000 description 1
BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
QCOGKXLOEWLIDC-UHFFFAOYSA-N N-methylbutylamine Chemical compound CCCCNC QCOGKXLOEWLIDC-UHFFFAOYSA-N 0.000 description 1
XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 1
PAMIQIKDUOTOBW-UHFFFAOYSA-N N-methylcyclohexylamine Natural products CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
230000003444 anaesthetic effect Effects 0.000 description 1
230000001773 anti-convulsant effect Effects 0.000 description 1
239000001961 anticonvulsive agent Substances 0.000 description 1
229960003965 antiepileptics Drugs 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000001816 cooling Methods 0.000 description 1
VXVVUHQULXCUPF-UHFFFAOYSA-N cycloheptanamine Chemical compound NC1CCCCCC1 VXVVUHQULXCUPF-UHFFFAOYSA-N 0.000 description 1
NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000007789 gas Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
230000000147 hypnotic effect Effects 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
NOBVTKCADZWKHR-UHFFFAOYSA-N n,2-dimethylprop-2-en-1-amine Chemical compound CNCC(C)=C NOBVTKCADZWKHR-UHFFFAOYSA-N 0.000 description 1
QKYWADPCTHTJHQ-UHFFFAOYSA-N n,2-dimethylpropan-1-amine Chemical compound CNCC(C)C QKYWADPCTHTJHQ-UHFFFAOYSA-N 0.000 description 1
JCBGGIHYIHYKEX-UHFFFAOYSA-N n-(2-methylprop-2-enyl)aniline Chemical compound CC(=C)CNC1=CC=CC=C1 JCBGGIHYIHYKEX-UHFFFAOYSA-N 0.000 description 1
RIWRFSMVIUAEBX-UHFFFAOYSA-N n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 description 1
IOXXVNYDGIXMIP-UHFFFAOYSA-N n-methylprop-2-en-1-amine Chemical compound CNCC=C IOXXVNYDGIXMIP-UHFFFAOYSA-N 0.000 description 1
GVWISOJSERXQBM-UHFFFAOYSA-N n-methylpropan-1-amine Chemical compound CCCNC GVWISOJSERXQBM-UHFFFAOYSA-N 0.000 description 1
DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 1
150000007530 organic bases Chemical group 0.000 description 1
IAWXHEPLJXAMSG-UHFFFAOYSA-N pent-2-en-1-amine Chemical compound CCC=CCN IAWXHEPLJXAMSG-UHFFFAOYSA-N 0.000 description 1
DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000010992 reflux Methods 0.000 description 1
BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
239000000932 sedative agent Substances 0.000 description 1
230000001624 sedative effect Effects 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH76960A 1960-01-27 1960-01-27 Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden CH376486A (de)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
CH76960A CH376486A (de)	1960-01-27	1960-01-27	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden
GB2902/61A GB906235A (en)	1960-01-27	1961-01-25	New aryloxy acetic acid amides and processes for their production
ES0264364A ES264364A2 (es)	1960-01-27	1961-01-26	Procedimiento para la preparaciën de nuevas amidas de acido ariloxiacetico
ES0264365A ES264365A2 (es)	1960-01-27	1961-01-26	Procedimiento para la preparaciën de amidas de acido ariloxiacetico
ES0264363A ES264363A1 (es)	1960-01-27	1961-01-26	Procedimiento para la preparaciën de nuevas amidas del acido ariloxiacetico
BE599535A BE599535A (fr)	1960-01-27	1961-01-26	Nouveaux amides d'acides aryloxyacétiques et leur préparation
FR859853A FR1093M (fr)	1960-01-27	1961-04-25	Médicament a base de dérivé d'acide phénoxy-acétique.

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH76960A CH376486A (de)	1960-01-27	1960-01-27	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden

Publications (1)

Publication Number	Publication Date
CH376486A true CH376486A (de)	1964-04-15

Family

ID=4194736

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH76960A CH376486A (de)	1960-01-27	1960-01-27	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden

Country Status (5)

Country	Link
BE (1)	BE599535A (fr)
CH (1)	CH376486A (fr)
ES (3)	ES264365A2 (fr)
FR (1)	FR1093M (fr)
GB (1)	GB906235A (fr)

1960
- 1960-01-27 CH CH76960A patent/CH376486A/de unknown
1961
- 1961-01-25 GB GB2902/61A patent/GB906235A/en not_active Expired
- 1961-01-26 ES ES0264365A patent/ES264365A2/es not_active Expired
- 1961-01-26 ES ES0264364A patent/ES264364A2/es not_active Expired
- 1961-01-26 ES ES0264363A patent/ES264363A1/es not_active Expired
- 1961-01-26 BE BE599535A patent/BE599535A/fr unknown
- 1961-04-25 FR FR859853A patent/FR1093M/fr active Active

Also Published As

Publication number	Publication date
ES264363A1 (es)	1961-07-16
GB906235A (en)	1962-09-19
BE599535A (fr)	1961-07-26
ES264365A2 (es)	1962-01-16
ES264364A2 (es)	1962-01-16
FR1093M (fr)	1962-01-29

Publication	Publication Date	Title
DE2141616C3 (de)	1975-04-10	Oxazole- und Oxazine eckige Klammer auf 3,2-c eckige Klammer zu chinazolinone, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
EP0153615A1 (fr)	1985-09-04	Procédé pour la préparation d'acide tétronique
DE1125428B (de)	1962-03-15	Verfahren zur Herstellung von 1-substituierten 3-Oxymethylpyrrolidinen
CH376486A (de)	1964-04-15	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden
DE1271116B (de)	1968-06-27	Verfahren zur Herstellung von 4-Hydroxypyrimidinen
AT223189B (de)	1962-09-10	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden
EP0284937A2 (fr)	1988-10-05	Procédé pour la fabrication d'acides gras 2-benzyliques
AT201586B (de)	1959-01-10	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden
EP0041923B1 (fr)	1984-03-07	Procédé pour la préparation de N-(1'-alcoxycarbonyléthyl)-2,6-dialkylanilines
DE1153375B (de)	1963-08-29	Verfahren zur Herstellung von Benzoxazin-(1, 3)-dionen-(2, 4)
AT222660B (de)	1962-08-10	Verfahren zur Herstellung von neuen Azepin-Derivaten
AT216504B (de)	1961-08-10	Verfahren zur Herstellung von neuen Isoindolinderivaten
AT214445B (de)	1961-04-10	Verfahren zur Herstellung von neuen, substituierten 1-(β-Oxyäthyl)-4-phenylpiperidinen
DE2331044A1 (de)	1974-01-10	Diphenylmethan-derivate und verfahren zu deren herstellung
AT208870B (de)	1960-05-10	Verfahren zur Herstellung von neuen N-substituierten Azepinen bzw. Dihydroazepinen
DE2854627B1 (de)	1979-10-04	Verfahren zur Herstellung von Aminocarbonsaeruehydrochloriden bzw. Diaminocarbonsaeure-di-hydrochloriden
DE2648944C3 (de)	1979-04-05	Verfahren zur Herstellung von N-Phenyl-5-chlor-2-nitranilin
AT211822B (de)	1960-11-10	Verfahren zur Herstellung von neuen Aryloxyessigsäureamiden
DE962336C (de)	1957-04-18	Verfahren zur Herstellung von basisch substituierten Carbonsaeureamiden
AT222104B (de)	1962-07-10	Verfahren zur Herstellung von neuen Cyclobutanderivaten
DE2103119A1 (en)	1972-07-27	N-substd-2,3-diphenyl-allylamines - prepn from the corresp alcohol via the bromide
DE2318024A1 (de)	1973-10-31	Verfahren zur herstellung von 2-phenylalkoxycarbonyl-tetrahydro-1,4-oxazinen
AT219611B (de)	1962-02-12	Verfahren zur Herstellung von neuen N-heterocyclischen Verbindungen und deren Salzen
AT300787B (de)	1972-08-10	Verfahren zur Herstellung von neuen 1-Aminoäthyl-indolderivaten und ihren Salzen
AT200134B (de)	1958-10-25	Verfahren zur Herstellung von a-Amino-b-oxycarbonsäureamiden