PL84340B1 - - Google Patents
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- Publication number
- PL84340B1 PL84340B1 PL17465570A PL17465570A PL84340B1 PL 84340 B1 PL84340 B1 PL 84340B1 PL 17465570 A PL17465570 A PL 17465570A PL 17465570 A PL17465570 A PL 17465570A PL 84340 B1 PL84340 B1 PL 84340B1
- Authority
- PL
- Poland
- Prior art keywords
- phenyl
- chlorine
- bromine
- compound
- substituted
- Prior art date
Links
- 238000000034 method Methods 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 3
- 229910052794 bromium Inorganic materials 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 230000002140 halogenating effect Effects 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- -1 hydroxy-thienyl group Chemical group 0.000 claims 2
- CHRAJVQLWOMYQI-SCZZXKLOSA-N (1s,5r)-5,8,8-trimethyl-3-azabicyclo[3.2.1]octane Chemical group C1NC[C@H]2CC[C@]1(C)C2(C)C CHRAJVQLWOMYQI-SCZZXKLOSA-N 0.000 claims 1
- SAKJVQIASONOAF-UHFFFAOYSA-N 4-(azepan-1-yl)morpholine Chemical compound C1COCCN1N1CCCCCC1 SAKJVQIASONOAF-UHFFFAOYSA-N 0.000 claims 1
- GZOYAPPUYJGHOC-UHFFFAOYSA-N Cl[IH]C1=CC=CC=C1 Chemical compound Cl[IH]C1=CC=CC=C1 GZOYAPPUYJGHOC-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Chemical group 0.000 claims 1
- 230000026030 halogenation Effects 0.000 claims 1
- 238000005658 halogenation reaction Methods 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Claims (4)
1. Zastrzezenia patentowe 1. Sposób wytwarzania nowych, zasadowo pod¬ stawionych trzeciorzedowych butanoli o wzorze 1, w którym Hal oznacza atom chloru lub bromu, Ri oznacza atom *vodoru, chloru lub bromu, R2 i R3 sa jednakowe lub rózne i oznaczaja proste lub rozgalezione grupy alkilowe, dwualkiloaminoalkilo- we, cykloalkilowe, fenylowe, aryloalkilowe lub ada1 mantylowe, przy czym jeden z symboli R2 lub R3 moze oznaczac takze atom wodoru, lub razem z atomem azotu oznaczaja ewentualnie podstawio¬ ny grupami hydroksylowymi, alkoksylowymi, fe- nylowymi lub nizszymi grupami alkilowymi, pier¬ scien pirolidynowy, piporydynowy, piperazynowy, morfolinowy, heksametylenoiminowy lub kamfidy- » nowy, a R4 oznacza prosta lub rozgaleziona grupe alkilowa, cykloalkilowa, norbornylowa, fenylowa, aralkilowa, naftylowa, pirydylowa lub tienylowa, podstawiona grupami hydroksylowymi lub nizszymi grupami alkilowymi grupe cykloalkilowa, lub pod- 10 stawiona grupami hydroksylowymi, alkilowymi, alkoksylowymi, alkilotiolowymi, trójfluorometylo- wymi, fenylowymi i fenoksylowymi lub atomami fluoru, chloru lub bromu grupe fenylowa, jak rów¬ niez ich fizjologicznie dopuszczalnych soli addy- 15 cyjnych z kwasami, znamienny tym, ze zwiazek o wzorze ogólnym 2, w którym Rj, R2, R3 i R4 maja wyzej podane znaczenie, chlorowcuje sie w obecnosci rozpuszczalnika, a otrzymany zwiazek o wzorze ogólnym 1 ewentualnie przeprowadza sie 20 w sól z fizjologicznie dopuszczalnym nieorganicz¬ nym lub organicznym kwasem.
2. Sposób wedlug zastrz. 1, znamienny tym, ze chlorowcowanie prowadzi sie w temperaturach od 0 do 50°C. 25
3. Sposób wedlug zastrz. 1 albo 2, znamienny tym, ze jako srodek chlorowcujacy stosuje sie chlor, chlorek sulfurylu, jodochlorek fenylowy, brom, bromek jodu lub nadbromek pirydyniowy.
4. Sposób wedlug zastrz. 1 albo 2, znamienny *o tym, ze na 1 mol zwiazku o wzorze ogólnym 2 stosuje sie 1 lub 2 mole srodka chlorowcujacego lub jego niewielki nadmiar.81310 OH I C-CH2-CH2-CH2-N, ,R~ ^R„ WZÓR 1 OH p JL / 2 C-CH2-CH2-CH2-Nx XR„ WZdR 2 O NH. C-R. R1 WZdR 3 CZV PL PL
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL17465570A PL84340B1 (pl) | 1970-10-12 | 1970-10-12 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL17465570A PL84340B1 (pl) | 1970-10-12 | 1970-10-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL84340B1 true PL84340B1 (pl) | 1976-03-31 |
Family
ID=19969190
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL17465570A PL84340B1 (pl) | 1970-10-12 | 1970-10-12 |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL84340B1 (pl) |
-
1970
- 1970-10-12 PL PL17465570A patent/PL84340B1/pl unknown
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