JP4479917B2

JP4479917B2 - イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤

イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 Download PDF

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Publication number: JP4479917B2
Authority: JP; Japan
Prior art keywords: alkyl; trifluoromethyl; dihydro; isoxazol; dichlorophenyl
Prior art date: 2005-09-02
Legal status : Active

Application number

JP2006237617A

Other languages

English (en)

Japanese (ja)

Other versions

JP2007308471A (ja

JP2007308471A5 (enExample

Inventor

猛志三田

隆正菊池

隆司水越

学八尾坂

充陽菰田

Current Assignee

Nissan Chemical Corp

Original Assignee

Nissan Chemical Corp

Priority date

2005-09-02

Filing date

2006-09-01

Publication date

2010-06-09

2006-09-01 Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp

2006-09-01 Priority to JP2006237617A priority Critical patent/JP4479917B2/ja

2007-11-29 Publication of JP2007308471A publication Critical patent/JP2007308471A/ja

2009-11-05 Publication of JP2007308471A5 publication Critical patent/JP2007308471A5/ja

2010-06-09 Application granted granted Critical

2010-06-09 Publication of JP4479917B2 publication Critical patent/JP4479917B2/ja

2026-09-01 Anticipated expiration legal-status Critical

Status Active legal-status Critical Current

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-1 Isoxazoline-substituted benzamide compounds Chemical class 0.000 title claims description 700
241000607479 Yersinia pestis Species 0.000 title claims description 26
239000000460 chlorine Substances 0.000 claims description 484
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 301
SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 276
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 266
125000000217 alkyl group Chemical group 0.000 claims description 206
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 202
125000005843 halogen group Chemical group 0.000 claims description 173
125000001309 chloro group Chemical group Cl* 0.000 claims description 132
125000004432 carbon atom Chemical group C* 0.000 claims description 125
125000004093 cyano group Chemical group *C#N 0.000 claims description 117
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 104
MNLAVFKVRUQAKW-UHFFFAOYSA-N VR nerve agent Chemical compound CCN(CC)CCSP(C)(=O)OCC(C)C MNLAVFKVRUQAKW-UHFFFAOYSA-N 0.000 claims description 100
125000004433 nitrogen atom Chemical group N* 0.000 claims description 92
RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical group FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 88
229910052757 nitrogen Inorganic materials 0.000 claims description 86
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 80
VOUMVHRRAVBACH-RXCQEBQVSA-N quinocarcin Chemical compound C=1([C@@H]2CO[C@H]3N42)C(OC)=CC=CC=1C[C@H]4[C@@H]1N(C)[C@H]3C[C@H]1C(O)=O VOUMVHRRAVBACH-RXCQEBQVSA-N 0.000 claims description 76
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 72
229910052799 carbon Inorganic materials 0.000 claims description 66
125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 64
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 61
229910052717 sulfur Inorganic materials 0.000 claims description 61
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 59
125000002947 alkylene group Chemical group 0.000 claims description 59
125000004434 sulfur atom Chemical group 0.000 claims description 57
125000004430 oxygen atom Chemical group O* 0.000 claims description 55
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 53
GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 claims description 49
125000001188 haloalkyl group Chemical group 0.000 claims description 45
125000004429 atom Chemical group 0.000 claims description 42
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 41
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 39
125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 38
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 37
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 37
SVSARCCKBMZNMR-UHFFFAOYSA-N [1-[2-[methyl-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethyl]amino]ethyl]pyridin-4-ylidene]methyl-oxoazanium;dichloride Chemical compound [Cl-].[Cl-].C1=CC(=C[NH+]=O)C=CN1CCN(C)CCN1C=CC(=C[NH+]=O)C=C1 SVSARCCKBMZNMR-UHFFFAOYSA-N 0.000 claims description 37
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 36
150000003839 salts Chemical class 0.000 claims description 36
125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 33
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 33
125000003342 alkenyl group Chemical group 0.000 claims description 32
125000000304 alkynyl group Chemical group 0.000 claims description 32
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 30
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 28
125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 27
125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 26
125000005347 halocycloalkyl group Chemical group 0.000 claims description 26
239000003795 chemical substances by application Substances 0.000 claims description 25
VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 23
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 23
125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims description 22
125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 21
QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 claims description 21
125000001424 substituent group Chemical group 0.000 claims description 21
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 20
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 20
101150065749 Churc1 gene Proteins 0.000 claims description 20
102100038239 Protein Churchill Human genes 0.000 claims description 20
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 19
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
238000000034 method Methods 0.000 claims description 18
125000004043 oxo group Chemical group O=* 0.000 claims description 17
125000003545 alkoxy group Chemical group 0.000 claims description 16
KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 16
229910052801 chlorine Inorganic materials 0.000 claims description 16
125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 15
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 14
125000006772 (C1-C6) haloalkylsulfonyloxy group Chemical group 0.000 claims description 14
125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 14
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
125000000464 thioxo group Chemical group S=* 0.000 claims description 14
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 11
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 claims description 11
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
239000001301 oxygen Substances 0.000 claims description 10
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 9
241000124008 Mammalia Species 0.000 claims description 9
239000004480 active ingredient Substances 0.000 claims description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 8
229910052740 iodine Inorganic materials 0.000 claims description 8
AJIPIJNNOJSSQC-NYLIRDPKSA-N estetrol Chemical group OC1=CC=C2[C@H]3CC[C@](C)([C@H]([C@H](O)[C@@H]4O)O)[C@@H]4[C@@H]3CCC2=C1 AJIPIJNNOJSSQC-NYLIRDPKSA-N 0.000 claims description 7
125000000623 heterocyclic group Chemical group 0.000 claims description 7
239000002917 insecticide Substances 0.000 claims description 7
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
125000004775 chlorodifluoromethyl group Chemical group FC(F)(Cl)* 0.000 claims description 6
125000000232 haloalkynyl group Chemical group 0.000 claims description 6
125000001624 naphthyl group Chemical group 0.000 claims description 5
241001465754 Metazoa Species 0.000 claims description 4
230000000895 acaricidal effect Effects 0.000 claims description 4
244000078703 ectoparasite Species 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
239000000642 acaricide Substances 0.000 claims description 3
239000003905 agrochemical Substances 0.000 claims description 3
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 3
125000004692 haloalkylcarbonyl group Chemical group 0.000 claims description 3
244000144972 livestock Species 0.000 claims description 3
244000045947 parasite Species 0.000 claims description 3
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 2
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims description 2
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 2
125000003971 isoxazolinyl group Chemical group 0.000 claims description 2
125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 2
125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 claims description 2
238000005406 washing Methods 0.000 claims description 2
125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 claims 89
125000006479 2-pyridyl methyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims 4
239000000546 pharmaceutical excipient Substances 0.000 claims 3
125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims 2
MWDZXUOUTGAFAL-UHFFFAOYSA-N n-(2,2,2-trifluoroethyl)benzamide Chemical compound FC(F)(F)CNC(=O)C1=CC=CC=C1 MWDZXUOUTGAFAL-UHFFFAOYSA-N 0.000 claims 2
JHBTVPLZRMXZKD-UHFFFAOYSA-N n-(pyridin-2-ylmethyl)benzamide Chemical compound C=1C=CC=CC=1C(=O)NCC1=CC=CC=N1 JHBTVPLZRMXZKD-UHFFFAOYSA-N 0.000 claims 2
238000007911 parenteral administration Methods 0.000 claims 2
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims 1
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims 1
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 1
125000006305 3-iodophenyl group Chemical group [H]C1=C([H])C(I)=C([H])C(*)=C1[H] 0.000 claims 1
BUSYZRSTDLGCPA-UHFFFAOYSA-N 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n',2-dimethyl-n'-phenylbenzohydrazide Chemical compound C=1C=CC=CC=1N(C)NC(=O)C(C(=C1)C)=CC=C1C(C1)=NOC1(C(F)(F)F)C1=CC(Cl)=CC(Cl)=C1 BUSYZRSTDLGCPA-UHFFFAOYSA-N 0.000 claims 1
CUMQZYNQYJFUGP-UHFFFAOYSA-N 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[2-(dimethylamino)-2-oxoethyl]-2-methylbenzamide Chemical compound C1=C(C)C(C(=O)NCC(=O)N(C)C)=CC=C1C1=NOC(C(F)(F)F)(C=2C=C(Cl)C=C(Cl)C=2)C1 CUMQZYNQYJFUGP-UHFFFAOYSA-N 0.000 claims 1
ZJJZVFYCXHWSOI-UHFFFAOYSA-N 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[2-(ethylamino)-2-oxoethyl]-2-methylbenzamide Chemical compound C1=C(C)C(C(=O)NCC(=O)NCC)=CC=C1C1=NOC(C(F)(F)F)(C=2C=C(Cl)C=C(Cl)C=2)C1 ZJJZVFYCXHWSOI-UHFFFAOYSA-N 0.000 claims 1
125000006306 4-iodophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1I 0.000 claims 1
NWMMMISKPBXNRM-UHFFFAOYSA-N ClC1=CC=C(C=N1)CNC(C1=C(C=C(C=C1)C1=NOC(C1)(C(F)(F)F)C1=CC(=CC(=C1)Cl)Cl)C)=O Chemical compound ClC1=CC=C(C=N1)CNC(C1=C(C=C(C=C1)C1=NOC(C1)(C(F)(F)F)C1=CC(=CC(=C1)Cl)Cl)C)=O NWMMMISKPBXNRM-UHFFFAOYSA-N 0.000 claims 1
XCUAIINAJCDIPM-XVFCMESISA-N N(4)-hydroxycytidine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=NO)C=C1 XCUAIINAJCDIPM-XVFCMESISA-N 0.000 claims 1
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
DGYIJVNZSDYBOE-UHFFFAOYSA-N [CH2]C1=CC=NC=C1 Chemical group [CH2]C1=CC=NC=C1 DGYIJVNZSDYBOE-UHFFFAOYSA-N 0.000 claims 1
238000003287 bathing Methods 0.000 claims 1
GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims 1
238000010410 dusting Methods 0.000 claims 1
244000079386 endoparasite Species 0.000 claims 1
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
238000007654 immersion Methods 0.000 claims 1
238000010255 intramuscular injection Methods 0.000 claims 1
239000007927 intramuscular injection Substances 0.000 claims 1
239000007928 intraperitoneal injection Substances 0.000 claims 1
238000010253 intravenous injection Methods 0.000 claims 1
FGEAHGNDNXEVKA-UHFFFAOYSA-N methyl n-[4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-2-methylbenzoyl]-n-(n-methylanilino)carbamate Chemical compound C=1C=C(C=2CC(ON=2)(C=2C=C(Cl)C=C(Cl)C=2)C(F)(F)F)C=C(C)C=1C(=O)N(C(=O)OC)N(C)C1=CC=CC=C1 FGEAHGNDNXEVKA-UHFFFAOYSA-N 0.000 claims 1
HGTGCLBXLPLRNB-UHFFFAOYSA-N n-(3,3,3-trifluoropropyl)benzamide Chemical compound FC(F)(F)CCNC(=O)C1=CC=CC=C1 HGTGCLBXLPLRNB-UHFFFAOYSA-N 0.000 claims 1
VDJSXBBFSHLEHE-UHFFFAOYSA-N n-(pyridin-4-ylmethyl)benzamide Chemical compound C=1C=CC=CC=1C(=O)NCC1=CC=NC=C1 VDJSXBBFSHLEHE-UHFFFAOYSA-N 0.000 claims 1
SQVQOCWOZHALQO-UHFFFAOYSA-N n-acetyl-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n',2-dimethyl-n'-phenylbenzohydrazide Chemical compound C=1C=CC=CC=1N(C)N(C(C)=O)C(=O)C(C(=C1)C)=CC=C1C(C1)=NOC1(C(F)(F)F)C1=CC(Cl)=CC(Cl)=C1 SQVQOCWOZHALQO-UHFFFAOYSA-N 0.000 claims 1
OCAAZRFBJBEVPS-UHFFFAOYSA-N prop-2-enyl carbamate Chemical compound NC(=O)OCC=C OCAAZRFBJBEVPS-UHFFFAOYSA-N 0.000 claims 1
238000005507 spraying Methods 0.000 claims 1
238000010254 subcutaneous injection Methods 0.000 claims 1
239000007929 subcutaneous injection Substances 0.000 claims 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1332
150000001875 compounds Chemical class 0.000 description 124
238000006243 chemical reaction Methods 0.000 description 66
150000001721 carbon Chemical group 0.000 description 53
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 42
125000000753 cycloalkyl group Chemical group 0.000 description 34
239000002904 solvent Substances 0.000 description 33
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 30
JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 description 29
125000006412 propinylene group Chemical group [H]C#CC([H])([H])* 0.000 description 25
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 21
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
239000002585 base Substances 0.000 description 20
238000004519 manufacturing process Methods 0.000 description 20
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 19
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 18
125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 description 18
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 16
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 16
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 15
XSXHWVKGUXMUQE-UHFFFAOYSA-N osmium dioxide Inorganic materials O=[Os]=O XSXHWVKGUXMUQE-UHFFFAOYSA-N 0.000 description 15
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 15
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 14
125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 14
DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 description 13
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 12
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 12
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 12
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 11
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 11
XPHBRTNHVJSEQD-UHFFFAOYSA-N anidoxime Chemical group C=1C=CC=CC=1C(CCN(CC)CC)=NOC(=O)NC1=CC=C(OC)C=C1 XPHBRTNHVJSEQD-UHFFFAOYSA-N 0.000 description 11
125000004438 haloalkoxy group Chemical group 0.000 description 11
150000002430 hydrocarbons Chemical group 0.000 description 11
238000010992 reflux Methods 0.000 description 11
239000000758 substrate Substances 0.000 description 11
125000003118 aryl group Chemical group 0.000 description 10
ZJULYDCRWUEPTK-UHFFFAOYSA-N dichloromethyl Chemical compound Cl[CH]Cl ZJULYDCRWUEPTK-UHFFFAOYSA-N 0.000 description 10
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