CA2399183A1

CA2399183A1 - Thioimidazolidine derivatives

Thioimidazolidine derivatives Download PDF

Info

Publication number: CA2399183A1
Authority: CA; Canada
Prior art keywords: independently; substituted; another; c4alkyl; unsubstituted
Prior art date: 2000-02-25
Legal status : Abandoned

Application number

CA002399183A

Other languages

English (en)

French (fr)

Inventor

Dario Lazzari

Graziano Zagnoni

Current Assignee

BASF Schweiz AG

Original Assignee

Individual

Priority date

2000-02-25

Filing date

2001-02-19

Publication date

2001-08-30

2001-02-19 Application filed by Individual filed Critical Individual

2001-08-30 Publication of CA2399183A1 publication Critical patent/CA2399183A1/en

Status Abandoned legal-status Critical Current

Links

-1 C1-C18alkyl Chemical group 0.000 claims abstract description 136
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 136
150000001875 compounds Chemical class 0.000 claims abstract description 134
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 64
239000001257 hydrogen Substances 0.000 claims abstract description 63
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 47
229910052799 carbon Inorganic materials 0.000 claims abstract description 43
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims abstract description 42
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 33
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 23
239000011368 organic material Substances 0.000 claims abstract description 21
230000003647 oxidation Effects 0.000 claims abstract description 7
238000007254 oxidation reaction Methods 0.000 claims abstract description 7
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 6
230000015556 catabolic process Effects 0.000 claims abstract description 6
238000006731 degradation reaction Methods 0.000 claims abstract description 6
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims abstract description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
230000000087 stabilizing effect Effects 0.000 claims abstract description 4
239000000203 mixture Substances 0.000 claims description 73
150000002431 hydrogen Chemical group 0.000 claims description 55
239000000463 material Substances 0.000 claims description 51
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NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 23
229910052757 nitrogen Inorganic materials 0.000 claims description 23
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 22
238000000034 method Methods 0.000 claims description 22
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IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 13
125000003118 aryl group Chemical group 0.000 claims description 11
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 9
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