ES448772A1 - Procedimiento para la obtencion de derivados de tiazinas. - Google Patents

Procedimiento para la obtencion de derivados de tiazinas.

Info

Publication number: ES448772A1
Authority: ES; Spain
Prior art keywords: arylthio; alkylthio; aryloxy; alkoxy; aryl
Prior art date: 1976-06-10
Legal status (The legal status 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 status listed.): Expired

Application number

ES448772A

Other languages

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Patronato de Investigacion Cientifica y Tecnica

Original Assignee

Patronato de Investigacion Cientifica y Tecnica

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.)

1976-06-10

Filing date

1976-06-10

Publication date

1977-07-16

1976-06-10 Application filed by Patronato de Investigacion Cientifica y Tecnica filed Critical Patronato de Investigacion Cientifica y Tecnica

1976-06-10 Priority to ES448772A priority Critical patent/ES448772A1/es

1977-07-16 Publication of ES448772A1 publication Critical patent/ES448772A1/es

Status Expired legal-status Critical Current

Links

238000000034 method Methods 0.000 title abstract 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
125000003545 alkoxy group Chemical group 0.000 abstract 3
125000004414 alkyl thio group Chemical group 0.000 abstract 3
125000003118 aryl group Chemical group 0.000 abstract 3
125000005110 aryl thio group Chemical group 0.000 abstract 3
125000004104 aryloxy group Chemical group 0.000 abstract 3
239000002904 solvent Substances 0.000 abstract 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
125000000217 alkyl group Chemical group 0.000 abstract 2
125000004659 aryl alkyl thio group Chemical group 0.000 abstract 2
125000002102 aryl alkyloxo group Chemical group 0.000 abstract 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
238000006243 chemical reaction Methods 0.000 abstract 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 abstract 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
-1 benzylthio Chemical group 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
125000005843 halogen group Chemical group 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
150000002431 hydrogen Chemical class 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1

Landscapes

Plural Heterocyclic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

ES448772A 1976-06-10 1976-06-10 Procedimiento para la obtencion de derivados de tiazinas. Expired ES448772A1 (es)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
ES448772A ES448772A1 (es)	1976-06-10	1976-06-10	Procedimiento para la obtencion de derivados de tiazinas.

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
ES448772A ES448772A1 (es)	1976-06-10	1976-06-10	Procedimiento para la obtencion de derivados de tiazinas.

Publications (1)

Publication Number	Publication Date
ES448772A1 true ES448772A1 (es)	1977-07-16

Family

ID=8471746

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES448772A Expired ES448772A1 (es)	1976-06-10	1976-06-10	Procedimiento para la obtencion de derivados de tiazinas.

Country Status (1)

Country	Link
ES (1)	ES448772A1 (es)

1976
- 1976-06-10 ES ES448772A patent/ES448772A1/es not_active Expired

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Legal Events

Date	Code	Title	Description
1997-08-01	FD1A	Patent lapsed	Effective date: 19970612