184138. lajstromszámú szabadalom • Hatóanyagként tiofoszforsav-észter amid-származékokat tartalmazó növényvédő készítmény és eljárás a hatóantagok előállítására
184 138 11 12 I. Táblázat folytatása Példa és hatóanyag száma (R)n R2 R3 X np ill. Op. 19 2,3—Cl2-ch3 ■-NH-CH(CH3)2-C3H5 0 nD24:1.54 52 20 2,4—Cl2-CH3-nh-ch3-c2h5 0 nD24: 1.5 6 04 21 2,4-Cl2-CH3-NH-CH(CH3)2 ~C3HS 0 nD24: 1.5405 22 2,4-CIj “CH3 -nh-ch2 -ch=ch2-C3HS 0 nD24: 1.5542 23 2,4-Cl2-CH3-NH-C4H9 (n)-C3HS 0 nD24: 1.5447 24 2,5—Cl2-CH3-NH-CH3-C3HS 0 nD24: 1.5645 25 2,5—Cl2-ch3-NH-CH(CH3)2-C3HS 0 nD24: 1.5502 26 2,5—Cl2-CH3 -nh-ch2-ch=ch2-C3HS 0 nD24: 1.5 5 97 27 2,5—Cl2-CH3-NH-C4H9 (n)-C3H5 0 nD24: 1.5474 28 3,4—Cl2-CH3-nh-ch3-C3HS 0 nD24: 1.5620 29 3,4—Cl2-CH3-NH-CH(CH3)2-C3H5 0 nD24: 1.5451 30 3,4-Cl2-ch3-NH-C4H9 (n)-C3HS 0 nDM: 1.5495 31 4-CH(CH3)2 —CH(CH3)2-nh-ch3-C3HS 0 nD24: 1.5226 32 4-CH(CH3)2-CH(CH3)2-NH-CH(CH3)2-C3HS 0 nD24: 1.5170 33 3-CF3-CH(CH3)2-NH-CH3-C3HS 0 nD24: 1.4980 34 3-CF3-CH(CH3)2-N(CH3)2-C3H5 0 nD24: 1.4935 35 3-CF3-CH(CH3)2-NH-CH(CH3)2-C3HS 0 nD24: 1.4953 36 3—CFj -C4H9 (szék)-nh-ch3-C3H5 0 nD24: 1.4994 37 3-CF3 -C4H9 (szék)-n(ch3)2 0 nD24: 1.4930 38 3—CF3 -C4H9 (szék)-NH-CH(CH3)2-c2h5 0 nD24: 1.4953 39 3—CF3 -C4H9 (szék) —NH-CH —CH=CH. 2 2-C3H5 Q nD24: 1.5047 40 4—Cl-ch(ch3)2-nh-ch3-CH3 0-41 2—F-CH(CH3)2-NH-CH(CH3)2-C2HS 0 nD24: 1.5171 42 H H -NH-C3H7-ízo-c2hs 0 nQ30: 1.5666 43 H H —NFI—ciklohexil-C2HS 0 Op: 90-93 °C 45 H H morfolino-C2H5 0 nD29: 1.5 5 68 46 H-CH3 morfolino-C2H5 0 — 47 3-CH3-C3H7’ÍZ°-NH-C4H9 (n)-C2H5 0 nD29: 1.5236 48 4_CH3-ch(ch3)2-NH-C4H9 (n)-C2H5 0 Op: 59 -64 °C 49 4-CH3-CH(CH3)2 -nh-ch2 -ch=ch2-C2HS 0 nD29: 1.5362 50 2-CH3-CH(CH3)2 -NH-C3H7-ízo-C2HS 0 nD32: 1.5255 51 2-CH3-CH(CH3)2 —nh-ch2_ch=CH2-C2H5 0 nD2ï: 1.5375 52 2,5-Cl2-CH3-NH-CH(CH3)2-c2h5 s nD28: 1.5647 53 4—Cl-CH(CH3)2 —NH-eiklohexil-C2H5 0 — 54 3—Cl-CH3-NH-ciklohexil-C2H5 0 np30: 1.5475 55 3—Cl-CH3 piperidino-C2H5 0 nj^30: 1.5540 56 2,4-Cl2-ch3-nh-ch3-C2H5 0 nn24: 1.5604 57 H-CH3-NHC3H7-ízo-C2HS 0 nD27: 1.5472 58 3-CH3-CH(CH3)2-NHC3H7-ízo-c2hs 0 nD32: 1.5188 59. 3-CH3-CH(CH3)2-nhch2-ch=ch2-C2HS 0 nj-j30: 1.5343 60 3-CH3-CH(CH3)2 morfolino-C2H5 0 nD32: 1.5 3 50 61 4-CH3-CH(CH3)2 morfolino-C2H5 0 nD32: 1.5343 62 4-CH3-CH(CH3)2-NHC3H7-izo-C2H5 0 Op: 69-71 °C 63 2-CH3-CH(CH3)2-NHC. H -izo-c2hs 0 nD29: 1.5257 64 2-CH3-CH(CH3)2 morfolino-c2hs 0 nD32: 1.5337 65 3—Cl-ch3 morfolino-C2HS 0 nD27: 1.5550 66 2,4—Cl2-CH(CH3)2 —NH-ciklohexil-C2HS 0 Op: 90-94 °C 67 2,4-Clj-CH3 morfolino-c2hs 0 nD2 7:1.5551 1
