JP2004525800A5 - - Google Patents

Info

Publication number

JP2004525800A5

JP2004525800A5 JP2002578297A JP2002578297A JP2004525800A5 JP 2004525800 A5 JP2004525800 A5 JP 2004525800A5 JP 2002578297 A JP2002578297 A JP 2002578297A JP 2002578297 A JP2002578297 A JP 2002578297A JP 2004525800 A5 JP2004525800 A5 JP 2004525800A5

Authority

JP

Japan

Prior art keywords

propyl

butyl

ethyl

methyl

phenyl

Prior art date

2002-03-20

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.)

Pending

Links

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• -1 pyrrolidino, piperidino Chemical group 0.000 claims 173
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 87
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 85
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 85
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 67
• 229910052739 hydrogen Inorganic materials 0.000 claims 67
• 239000001257 hydrogen Substances 0.000 claims 67
• 150000002431 hydrogen Chemical class 0.000 claims 60
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 53
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 52
• 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 47
• 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 47
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 33
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 32
• 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 32
• 125000000217 alkyl group Chemical group 0.000 claims 29
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 29
• 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims 28
• GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 28
• 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims 28
• 125000003944 tolyl group Chemical group 0.000 claims 24
• 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 18
• 125000001309 chloro group Chemical group Cl* 0.000 claims 18
• 125000006413 ring segment Chemical group 0.000 claims 18
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 16
• 150000001450 anions Chemical class 0.000 claims 15
• 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 15
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 11
• 239000010410 layer Substances 0.000 claims 11
• 125000004093 cyano group Chemical group *C#N 0.000 claims 9
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 8
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
• 150000001768 cations Chemical class 0.000 claims 7
• 230000003287 optical effect Effects 0.000 claims 7
• 101000650578 Salmonella phage P22 Regulatory protein C3 Proteins 0.000 claims 6
• 101001040920 Triticum aestivum Alpha-amylase inhibitor 0.28 Proteins 0.000 claims 6
• DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical group [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 claims 5
• 125000001544 thienyl group Chemical group 0.000 claims 5
• 125000004190 benzothiazol-2-yl group Chemical group [H]C1=C([H])C([H])=C2N=C(*)SC2=C1[H] 0.000 claims 4
• 239000000758 substrate Substances 0.000 claims 4
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 3
• 239000011230 binding agent Substances 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• 239000011241 protective layer Substances 0.000 claims 2
• 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 2
• 101100129500 Caenorhabditis elegans max-2 gene Proteins 0.000 claims 1
• 101100083446 Danio rerio plekhh1 gene Proteins 0.000 claims 1
• 238000010521 absorption reaction Methods 0.000 claims 1
• 239000000654 additive Substances 0.000 claims 1
• 239000000543 intermediate Substances 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
• 239000002904 solvent Substances 0.000 claims 1
• 125000005425 toluyl group Chemical group 0.000 claims 1