184138. lajstromszámú szabadalom • Hatóanyagként tiofoszforsav-észter amid-származékokat tartalmazó növényvédő készítmény és eljárás a hatóantagok előállítására
184 138 13 14 I. Táblázat folytatása Példa és hatóanyag száma Wn R, r2 R3 X nj-j ill. Op. 68 3,4-Cl,-ch(ch3)2-NHC4H9-n-C3Hs 0 nD29: 1.5 4 02 69 3,4-Cl2-CH(CH3)2-NHC3H7-izo-CzHS 0 nD31: 1.5419 70 3—Cl-CH(CH3)2-NHC3H7ízo-C3H5 0 nD31: 1.5350 71 4—Br-CH(CH3)2-NHC3H7 -izo _C2 HS 0 Op: 85-86 °C 72 2,5—Cl2-CH(CH3)2 —NHC3H7 izo-C2H5 0 Op: 103-105 °C 73 4-N02-CH(CH3)2-NHC3H7-izo-c2h5 0 Op: 46-52 °C 74 4-N02-CH(CH3)2-NHC4H9 n-C2HS 0 Op: 69-71 °C 75 4-N02-CH(CH3)2 -nh-ch2 -ch=ch2-C2HS 0 nD32: 1.5549 76 4-N02-CH(CH3)2 piperidino-c2hs 0 nD32: 1.5483 77 4-SCH3-CH(CH3)2 —NHC3 H? izo-C2HS 0 Op: 81-84 °C 78 2,4-Cl2-CH3 -NHCH(CH3)2-C2HS 0 nD24: 1.5405 79 2,4-CIj-CH3 -nh-ch2 -ch=ch2-C2H5 0 nD24: 1.5542 80 3-CH3-CH(CH3)2 —NH-ciklohexil-c2hs 0 nD25: 1.5 3 70 81 3-CH3-CH(CH3)2 piperidino-C2H5 0 nD31: 1.5347 82 4-CH3-CH(CH3)2 —NH-ciklohexil-C2HS 0 Op: 74-75 °C 83 4-CH3-CH(CH3)2 piperidino-C2HS 0 nD31:1.5 340 84 4-SCH3-CH(CH3)2 —NHC H n-c2h5 0 Op: 65-67 °C 85 4-N02-CH(CH3)2 morfolino-C2H5 0 nD24: 1.5608 86 4-N02-C3HS —NHC H n 4 9-C2HS 0 Op: 75-76 °C 87 4-N02-CaHS morfolino-C2HS 0 nD27: 1.5620 88 3-N02-CH3-NHC3H7 iso C2 H5 0 nD27: 1.5519 89 3-N02-CH3 -NH-CH —CH=CH “C2H5 0 Op: 86-87 °C 90 3-N02-CH3 morfolino-C2HS 0 nD27: 1.5622 91 3-cr-CH3-NHC3H7-izo-C2HS s nD28: 1.5752 92 2,5—CÍ2-CH3-NHC3H7 izo-C2H5 s nD28 : 1.5647 93 2,4,6-Cl3 H-NHC3H7 izo-c2h5 0 nD23: 1.561 94 2,4,6-Cl3 H -nh-ch2 -ch=ch2-C2HS 0 Op: 55-57 °C 95 2,4,6—Cl3 H-NHC4H9 n-C2H5 0 Op: 82-85 °C 96 3,4,5—Cl3 H-NHC3H7 izo-C2HS 0 Op: 168-171 °C 97 3,4,5—Cl3 H -nh-ch2 -ch=ch2-C2H5 0 Op: 119-121 °C 98 3,4,5—Cl3 H-NHC. H n-C2H5 0 Op: 93-96 °C 99 3,4,5 -Cl3-CH3-NHC3H7-izo-c2hs 0 Op: 84-87 °C 100 3,4,5—Cl3-CH3-NHC. H„ -n-C2H5 0 nD23: 1.5 5 94 101 2-CH3-ch(ch3)2 piperidino~C2HS 0 nD28: 1.5 3 60 102 H-CH(CH3)2-NHC3H7-n-c2h5 s Op: 76-78 °C 103 2—N02-ch3-n(ch3)2-C2H5 0 nD26: 1.5460 104 2-N02-CH3-nhch3-c2hs 0 nD26: 1.5538 105 2—N02-CH3 -NHCH(CH3)2-C2H5 0 nD26: 1.54 70 106 2—N02-CH3-nhch3-ch3 0 nD26: 1.5601 107 2—N02-ch3-N(CH3)2-ch3 0 nD26: 1.5592 108 2—N02-CH3 -NHCH(CH3)2-CH3 0 nD26: 1.5482 109 3-CH3-C2HS-NHC3H7 -izo-c2h5 0 nD25: 1.53 1 3 110 3—CH3-C3Hs-nhch3-C2H5 0 nD25: 1.5 3 9 5 111 2—CH3-c2h5-NHC3H7-ízo-c2h5 0 nD24: 1.5310 112 4-CH3-CH3-NHC3H7-ízo-C2H5 0 nD24: 1.5385 113 4-CH3-c2h5-nhch3-C2H5 0 nD24: 1.5402 114 4-CH3-C,Hs-NHC3H7-ízo-c2h5 0 nD24: 1.5300 115 2-CH3-c2h5-nhch3-c2h5 0 nD24: 1.5407 8
