SU368745A1 - - Google Patents

Info

Publication number

SU368745A1

SU368745A1 SU51007A SU51007A SU368745A1 SU 368745 A1 SU368745 A1 SU 368745A1 SU 51007 A SU51007 A SU 51007A SU 51007 A SU51007 A SU 51007A SU 368745 A1 SU368745 A1 SU 368745A1

Authority

SU

USSR - Soviet Union

Prior art keywords

general formula

urea

nhr

alkenyl

residue

Prior art date

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• -1 cycloheptyl ethyl Chemical group 0.000 description 8
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
• 238000000034 method Methods 0.000 description 6
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
• 125000000217 alkyl group Chemical group 0.000 description 4
• 150000008064 anhydrides Chemical class 0.000 description 4
• 150000003839 salts Chemical class 0.000 description 4
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
• 125000002252 acyl group Chemical group 0.000 description 3
• 125000003342 alkenyl group Chemical group 0.000 description 3
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
• 239000002253 acid Substances 0.000 description 2
• 229910021529 ammonia Inorganic materials 0.000 description 2
• 125000004429 atom Chemical group 0.000 description 2
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
• 229910052799 carbon Inorganic materials 0.000 description 2
• 125000004432 carbon atom Chemical group C* 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 2
• 150000002148 esters Chemical class 0.000 description 2
• 150000004820 halides Chemical class 0.000 description 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
• 238000002360 preparation method Methods 0.000 description 2
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
• 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
• 241001649081 Dina Species 0.000 description 1
• 239000003513 alkali Substances 0.000 description 1
• 125000002947 alkylene group Chemical group 0.000 description 1
• GHDLZGOOOLEJKI-UHFFFAOYSA-N benzenesulfonylurea Chemical compound NC(=O)NS(=O)(=O)C1=CC=CC=C1 GHDLZGOOOLEJKI-UHFFFAOYSA-N 0.000 description 1
• 230000004071 biological effect Effects 0.000 description 1
• 125000004093 cyano group Chemical group *C#N 0.000 description 1
• 125000000753 cycloalkyl group Chemical group 0.000 description 1
• 125000006622 cycloheptylmethyl group Chemical group 0.000 description 1
• 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
• WUESWDIHTKHGQA-UHFFFAOYSA-N cyclohexylurea Chemical group NC(=O)NC1CCCCC1 WUESWDIHTKHGQA-UHFFFAOYSA-N 0.000 description 1
• 125000006623 cyclooctylmethyl group Chemical group 0.000 description 1
• 229940058172 ethylbenzene Drugs 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 230000020477 pH reduction Effects 0.000 description 1
• 125000003884 phenylalkyl group Chemical group 0.000 description 1
• 238000001953 recrystallisation Methods 0.000 description 1
• 238000000926 separation method Methods 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• 125000001424 substituent group Chemical group 0.000 description 1
• 239000000725 suspension Substances 0.000 description 1
• XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1